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NCT Number: NCT04573660

Abbott Vascular Medical Device Registry

The AV-MDR is a prospective, non-randomized, open-label, multi-center registry. The purpose of the AV-MDR study is to proactively collect and evaluate clinical data on the usage of the devices in scope within their intended use with the aim of confirming safety and performance throughout their expected lifetime, ensuring the continued acceptability of identified risks, detecting emerging risks on the basis of factual evidence, ensuring the continued acceptability of the benefit-risk ratio, and identifying possible systematic misuse or off-label usage such that the intended use can be verified as appropriate.

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Key information

Conditions

Acute Myocardial Infarction Amino Acid Metabolism, Inborn Errors Arterial Embolism Brain Diseases Brain Diseases, Metabolic Brain Diseases, Metabolic, Inborn Cardiovascular Diseases Central Nervous System Diseases Congenital, Hereditary, and Neonatal Diseases and Abnormalities Coronary Artery Lesions Coronary Disease Coronary Restenosis Coronary Stenosis Genetic Diseases, Inborn Genetic Diseases, X-Linked Heart Diseases Metabolic Diseases Metabolism, Inborn Errors Myocardial Ischemia Nervous System Diseases Nutritional and Metabolic Diseases Ornithine Carbamoyltransferase Deficiency Disease Restenoses, Coronary Urea Cycle Disorders, Inborn Vascular Diseases Venous Embolism

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Perth Institute of Vascular Research, Nedlands, WAUS, Australia

Loading trial locations.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Subject is at least 18 years of age.
  • Subject has a planned procedure, or underwent a procedure, that will use/used one or more Abbott target devices covered in this registry.
  • Subject is willing and able to comply with, or has already completed, the follow-up schedule specified in this protocol.
  • Subject must provide written informed consent prior to any clinical investigation-related data collection or be enrolled under an IRB/EC approved waiver of consent.

Exclusion criteria

  • Subject has active symptoms and/or a positive test result of COVID-19 or other rapidly spreading novel infectious agent within the prior 2 months of the date of procedure.

Treatment and study plan

Coronary and peripheral stents

Device

The participants in the Coronary and peripheral stents arm will receive Coronary and peripheral stents

Pacing catheters

Device

The participants in the Pacing catheters arm will receive Pacing catheters

Vascular plugs

Device

The participants in the Vascular plugs arm will receive Vascular plugs

Measurement and imaging (FFR and OCT)

Device

The participants in the Measurement and imaging (FFR and OCT) arm will receive Measurement and imaging (FFR and OCT)

Peripheral dilatation catheters

Device

The participants in the Peripheral dilatation catheters will receive Peripheral dilatation catheters

Coronary dilatation catheters

Device

The participants in the Coronary dilatation catheters will receive Coronary dilatation catheters

Coronary and peripheral guidewires

Device

The participants in the Coronary and peripheral guidewires will receive Coronary and peripheral guidewires

Vessel closure/compression devices

Device

The participants in the Vessel closure/compression devices will receive Vessel closure/compression devices

Vascular access introducers

Device

The participants in the Vascular access introducers arm will receive Vascular access introducers

Primary outcomes

  1. Coronary Stents - Number of participants with composite of all-cause death, MI or target lesion revascularization (TLR)

    Time frame: During procedure (Start of procedure: defined as time a guidewire first enters the vasculature. End of procedure: defined as vessel closure following the index procedure)

    Composite of all-cause death, MI or target lesion revascularization (TLR) will be assessed among the patients who receive Coronary Stents.

  2. Coronary Stents - Number of participants with composite of all-cause death, MI or target lesion revascularization (TLR)

    Time frame: 30 days

    Composite of all-cause death, MI or target lesion revascularization (TLR) will be assessed among the patients who receive Coronary Stents.

  3. Coronary Stents - Number of participants with composite of all-cause death, MI or target lesion revascularization (TLR)

    Time frame: 12 months

    Composite of all-cause death, MI or target lesion revascularization (TLR) will be assessed among the patients who receive Coronary Stents.

  4. Peripheral Stents - Number of participants with composite of all-cause death, amputation, and TLR

    Time frame: During procedure (Start of procedure: defined as time a guidewire first enters the vasculature. End of procedure: defined as vessel closure following the index procedure)

    Composite of all-cause death, amputation, and TLR will be assessed among the patients who receive Peripheral Stents.

  5. Peripheral Stents - Number of participants with composite of all-cause death, amputation, and TLR

    Time frame: 30 days

    Composite of all-cause death, amputation, and TLR will be assessed among the patients who receive Peripheral Stents.

  6. Peripheral Stents - Number of participants with composite of all-cause death, amputation, and TLR

    Time frame: 12 months

    Composite of all-cause death, amputation, and TLR will be assessed among the patients who receive Peripheral Stents.

  7. Peripheral Stents (Renal Indication) - Number of participants with composite of all-cause death, ipsilateral nephrectomy, Embolic events resulting in kidney damage or TLR

    Time frame: During procedure (Start of procedure: defined as time a guidewire first enters the vasculature. End of procedure: defined as vessel closure following the index procedure)

    Composite of all-cause death, ipsilateral nephrectomy, Embolic events resulting in kidney damage or TLR will be assessed among the patients who receive Peripheral Stents (Renal Indication).

  8. Peripheral Stents (Renal Indication) - Number of participants with composite of all-cause death, ipsilateral nephrectomy, Embolic events resulting in kidney damage or TLR

    Time frame: 30 days

    Composite of all-cause death, ipsilateral nephrectomy, Embolic events resulting in kidney damage or TLR will be assessed among the patients who receive Peripheral Stents (Renal Indication).

  9. Peripheral Stents (Renal Indication) - Number of participants with composite of TLR

    Time frame: 12 months

    Composite of TLR will be assessed among the patients who receive Peripheral Stents (Renal Indication).

  10. Pacing Catheters - Number of participants with composite of potential complications (venous thrombosis, pulmonary emboli, arrhythmias, perforation)

    Time frame: During procedure (Start of procedure: defined as time a guidewire first enters the vasculature. End of procedure: defined as vessel closure following the index procedure)

    Composite of potential complications (venous thrombosis, pulmonary emboli, arrhythmias, perforation) will be assessed among the patients who receive Pacing Catheters.

  11. Pacing Catheters - Loss of capture (assessed based on physiological parameter-ECG)

    Time frame: During procedure (Start of procedure: defined as time a guidewire first enters the vasculature. End of procedure: defined as vessel closure following the index procedure)

    Loss of capture (average time of loss of capture across patients) will be assessed among the patients who receive Pacing Catheters. ECG is used to measure whether the pacing device stimulates the heart. Absence of a stimulation is considered a loss of capture.

  12. Vascular Plugs - Number of participants with composite of potential complications (Implant success, occlusion success, migration)

    Time frame: During procedure (Start of procedure: defined as time a guidewire first enters the vasculature. End of procedure: defined as vessel closure following the index procedure)

    Composite of potential complications including implant success, occlusion success, migration will be assessed among the patients who receive Vascular Plugs.

  13. Vascular Plugs - Number of participants with composite of occlusion success and migration

    Time frame: 30 days

    Composite of occlusion success and migration will be assessed among the patients who receive Vascular Plugs.

  14. Fractional flow reserve - Number of participants with composite of vessel dissection, perforation, and thromboembolism

    Time frame: During procedure (Start of procedure: defined as time a guidewire first enters the vasculature. End of procedure: defined as vessel closure following the index procedure)

    Composite of vessel dissection, perforation, and thromboembolism during procedure will be assessed among the patients who receive Fractional flow reserve (FFR).

  15. Fractional flow reserve - Number of participants with signal drift (Signal drift between measurements (Pd/Pa** pressure drift >0.03; <0.97 or >1.03)

    Time frame: During procedure (Start of procedure: defined as time a guidewire first enters the vasculature. End of procedure: defined as vessel closure following the index procedure)

    Signal drift (Signal drift between measurements (Pd/Pa** pressure drift >0.03; <0.97 or >1.03) will be assessed among the patients who receive FFR.

  16. Optical Coherence Tomography Products - Number of participants with Intraprocedural complications (number of dissections ≥type B, slow flow or no reflow, thrombus, abrupt closure, perforation)

    Time frame: During procedure (Start of procedure: defined as time a guidewire first enters the vasculature. End of procedure: defined as vessel closure following the index procedure)

    Intraprocedural complications will be assessed among the patients who receive Optical Coherence Tomography (OCT).

  17. Optical Coherence Tomography Products - Number of participants with Successful crossing and image quality pre-PCI

    Time frame: During procedure - Before the stent is implanted (Start of procedure: defined as time a guidewire first enters the vasculature. End of procedure: defined as vessel closure following the index procedure)

    Successful crossing and image quality pre- PCI will be assessed among the patients who receive OCT.

  18. Optical Coherence Tomography Products - Number of participants with Successful crossing and image quality post-PCI

    Time frame: During procedure - Between 10-30 minutes post-PCI (Start of procedure: defined as time a guidewire first enters the vasculature. End of procedure: defined as vessel closure following the index procedure)

    Successful crossing and image quality post-PCI will be assessed among the patients who receive OCT.

  19. Peripheral Dilatation Catheters - Number of participants with Composite of major adverse events

    Time frame: During procedure (Start of procedure: defined as time a guidewire first enters the vasculature. End of procedure: defined as vessel closure following the index procedure)

    Composite of major adverse events (e.g., distal embolization, dissection, perforation, amputation primary to balloon usage, total occlusion, abrupt closure, renal failure primary to balloon usage will be assessed among the patients who receive Peripheral Dilatation Catheters.

  20. Peripheral Dilatation Catheters - Number of participants with Device success (Successful delivery, Successful inflation, Successful deflation, Successful withdrawal) (assessed based on physiological parameters)

    Time frame: During procedure (Start of procedure: defined as time a guidewire first enters the vasculature. End of procedure: defined as vessel closure following the index procedure)

    Device success (Successful delivery, Successful inflation, Successful deflation, Successful withdrawal) will be assessed among the patients who receive Peripheral Dilatation Catheters. Device success can be summarized as the successful treatment with the device.

  21. Coronary Guidewires - Number of participants with Composite of major adverse events

    Time frame: During procedure (Start of procedure: defined as time a guidewire first enters the vasculature. End of procedure: defined as vessel closure following the index procedure)

    Composite of major adverse events (e.g., vessel perforation, dissection, occlusion, embolism) will be assessed among the patients who receive Coronary Guidewires.

  22. Coronary Guidewires - Number of participants with Device success (Successfully placed, Successfully introduce/position diagnostic/interventional device, Successfully reach/cross target lesion) (assessed based on physiological parameters)

    Time frame: During procedure (Start of procedure: defined as time a guidewire first enters the vasculature. End of procedure: defined as vessel closure following the index procedure)

    Device success (Successfully placed, Successfully introduce/position diagnostic/interventional device, Successfully reach/cross target lesion will be assessed among the patients who receive Coronary Guidewires. Device success can be summarized as the successful treatment with the device.

  23. Peripheral Guidewires - Number of participants with Composite of major adverse events

    Time frame: During procedure (Start of procedure: defined as time a guidewire first enters the vasculature. End of procedure: defined as vessel closure following the index procedure)

    Composite of major adverse events (e.g., vessel perforation, dissection, occlusion, embolism) will be assessed among the patients who receive Peripheral Guidewires.

  24. Peripheral Guidewires - Number of participants with Device success (Successfully placed, Successfully introduce/position diagnostic/interventional device, Successfully reach/cross target lesion) (assessed based on physiological parameters)

    Time frame: During procedure (Start of procedure: defined as time a guidewire first enters the vasculature. End of procedure: defined as vessel closure following the index procedure)

    Device success (Successfully placed, Successfully introduce/position diagnostic/interventional device, Successfully reach/cross target lesion will be assessed among the patients who receive Peripheral Guidewires. Device success can be summarized as the successful treatment with the device.

  25. Coronary Dilatation Catheters - Number of participants with Composite of major adverse events

    Time frame: During procedure (Start of procedure: defined as time a guidewire first enters the vasculature. End of procedure: defined as vessel closure following the index procedure)

    Composite of major adverse events (e.g., distal embolization, dissection, perforation, amputation primary to balloon usage, total occlusion, abrupt closure, renal failure primary to balloon usage will be assessed among the patients who receive Coronary Dilatation Catheters.

  26. Coronary Dilatation Catheters - Number of participants with Device success (Successful delivery, Successful inflation, Successful deflation, Successful withdrawal) (assessed based on physiological parameters)

    Time frame: During procedure (Start of procedure: defined as time a guidewire first enters the vasculature. End of procedure: defined as vessel closure following the index procedure)

    Device success (Successful delivery, Successful inflation, Successful deflation, Successful withdrawal) will be assessed among the patients who receive Coronary Dilatation Catheters. Device success can be summarized as the successful treatment with the device.

  27. Vessel Closure Devices - Number of participants with Composite of access complications

    Time frame: During procedure (Start of procedure: defined as time a guidewire first enters the vasculature. End of procedure: defined as vessel closure following the index procedure)

    Composite of access complications (e.g., hematoma, stenosis/occlusion, infection, access site bleeding) will be assessed among the patients who receive Vessel Closure Devices.

  28. Vessel Closure Devices - Number of participants with Successful hemostasis Major and minor bleeding

    Time frame: During procedure (Start of procedure: defined as time a guidewire first enters the vasculature. End of procedure: defined as vessel closure following the index procedure)

    Successful hemostasis Major and minor bleeding will be assessed among the patients who receive Vessel Closure Devices.

  29. Vessel Compression Devices - Number of participants with Major and minor bleeding

    Time frame: During procedure (Start of procedure: defined as time a guidewire first enters the vasculature. End of procedure: defined as vessel closure following the index procedure)

    Major and minor bleeding will be assessed among the patients who receive Vessel Compression Devices.

  30. Vessel Compression Devices - Number of participants with Complications including: pseudoaneurysm, hematoma (>5cm) in diameter, Hb drop>20 g/L, extended compression time >6 hours, blood transfusion required, bleeding requiring surgical procedure

    Time frame: During procedure (Start of procedure: defined as time a guidewire first enters the vasculature. End of procedure: defined as vessel closure following the index procedure)

    Complications including: pseudoaneurysm requiring treatment, hematoma (>5cm) in diameter, Hb drop>20 g/L, extended compression time >6 hours, blood transfusion required, bleeding requiring surgical procedure will be assessed among the patients who receive Vessel Compression Devices.

  31. Vascular Access Introducers - Incidence of safety issues

    Time frame: During procedure (Start of procedure: defined as time a guidewire first enters the vasculature. End of procedure: defined as vessel closure following the index procedure)

    Incidence of safety issues (e.g., bleeding, air embolism, hematoma, vessel damage (dissection, perforation, pseudoaneurysm), infection, thrombosis, AV fistula, occlusion, radial artery spasm) will be assessed among the patients who receive Vascular Access Introducers.

  32. Vascular Access Introducers - Incidence of performance issues

    Time frame: During procedure (Start of procedure: defined as time a guidewire first enters the vasculature. End of procedure: defined as vessel closure following the index procedure)

    Incidence of performance issues (e.g., unable to introduce other devices, failure to maintain hemostasis valve integrity, air leakage, bending or kinking of introducer, difficulty inserting/removing the sheath, device breakage detachment or separation, issue with an associated accessory) will be assessed among the patients who receive Vascular Access Introducers.

Study contacts

Contact information is provided by the study sponsor or research team.

Chinedu Agbonghai, MS

CONTACT

[email protected]

Sharan Dhanjal, MPH

CONTACT

[email protected]

+1 714-926-8292

Sponsors and collaborators

Lead sponsor

Abbott Medical Devices

Industry

Registry information

Acronym: AV-MDR

Important dates

Study start
2020
Primary completion
2030
Study completion
2031
First posted
Oct 5, 2020
Registry last updated
Jul 3, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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