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NCT Number: NCT04971356

1-month DAPT Plus 5-month Ticagrelor Monotherapy Versus 12-month DAPT in Patients With Drug-coated Balloon

Drug-Coated Balloon (DCB) angioplasty is similar to plain old balloon angioplasty procedurally, but there is an anti-proliferative medication paclitaxel coated to the balloon. Treating ISR lesions with the DCB has the theoretical advantage of avoiding multiple stent layers and respecting the vessel anatomy. DCB has shown promising results for the treatment of ISR. Currently, DCB has a Class I indication to treat ISR recommended by European Society of Cardiology guidelines. In addition, some interventional cardiologist has also applied DCB in de novo lesions in their clinical practice.

Bleeding after PCI remains a substantial clinical problem. Bleeding post-PCI increases the risk of adverse outcomes such as death, non-fatal myocardial infarction, and prolongs hospital stay. Clinical data has suggested that major bleeding post-PCI would increase the risk of mortality 5.7-fold. The antiplatelet medications are the major cause of bleeding events post-PCI.

Current guidelines for stents recommended DAPT of aspirin plus a P2Y12 inhibitor for at least 12 months after stent implantation in patients with the acute coronary syndrome. Compared with the DES, because of the absence of metal inside the coronary artery, the use of DCB might theoretically allow shorter duration antiplatelet therapy. However, the optimal course of DAPT for the DCB treated patients remains controversial.

In 2013, the consensus from the German group suggested that for the acute coronary syndrome, DAPT should be used for 12 months. The consensus of DAPT developed by the European Society of Cardiology (ESC) in 2017 stated that "in patients treated with DCB, dedicated clinical trials investigating the optimal duration of DAPT are lacking." So far, there are no randomized data showing the optimal DAPT duration for the DCB treated patients.

In the current study, we use Aspirin + Ticagrelor for 1-month followed by Ticagrelor monotherapy for 5-month, afterward, Aspirin monotherapy for 6 months to be the antiplatelet regimen in the experimental arm, to compare with the Reference arm, which is Aspirin + Ticagrelor for 12-month in a non-inferiority statistical assumption, aiming to investigate the optimal duration of the DAPT in ACS patients after DCB treatment.

Active, Not Recruiting

This study is active but is not currently recruiting participants.

Key information

Age range

18 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Ling Tao

Xi'an, Shannxi, 710032, China

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Patients with an indication for PCI due to acute coronary syndrome
  • All target lesions can be successful treatment of PCI with drug-coated balloon (DCB)
  • Patients who are able to complete the follow-up and compliant to the prescribed medication

Exclusion criteria

  • Under the age of 18 or Older than 80 years old
  • Unable to give informed consent
  • Patient is a woman who is pregnant or nursing (a pregnancy test must be performed within 7 days prior to the index procedure in women of child-bearing potential according to local practice)
  • Known contraindication to medications such as Heparin, antiplatelet drugs, or contrast.
  • Currently participating in another trial and not yet at its primary endpoint
  • Planned elective surgery
  • Concurrent medical condition with a life expectancy of less than 1 years
  • Previous intracranial haemorrhage
  • Need long-term oral anticoagulant therapy
  • Cardiogenic shock
  • Previous stent implantation 6 month
  • In-stent thrombosis
  • Target lesion located in surgical conduit

Treatment and study plan

Aspirin 100mg for 1-month (immediately after PCI)

Drug

Aspirin for 1-month immediately after PCI to be a part of medication treatment in the Experimental arm

Ticagrelor 90mg for 6-month (immediately after PCI)

Drug

Ticagrelor for 6-month immediately after PCI to be a part of medication treatment in the Experimental arm

Aspirin 100mg for 6-month (6-month post PCI)

Drug

Aspirin for 6-month at 6 months post-PCI (after the discontinuation of the 6-month Ticagrelor treatment) to be a part of medication treatment in the Experimental arm

Aspirin 100mg for 12-month (immediately after PCI)

Drug

Aspirin for 12-month immediately after PCI to be a part of medication treatment in the Reference arm

Ticagrelor 90mg for 12-month (immediately after PCI)

Drug

Ticagrelor for 12-month immediately after PCI to be a part of medication treatment in the Reference arm

Primary outcomes

  1. Net adverse clinical events (NACE)

    Time frame: 12 months

    NACE is a composite clinical endpoint of all-cause death, any stroke, any MI, any revascularization and BARC type 3 or 5 bleeding events

Secondary outcomes

  1. Any ischemic or bleeding event

    Time frame: 1, 6 and 12 months

    Any ischemic and bleeding event includes any all-cause death, any stroke, MI, BARC-defined type 3 bleeding, any revascularization and BARC-defined type 2 bleeding events

  2. BARC type 3 or 5 bleeding events

    Time frame: 1, 6 and 12 months

    Bleeding events type 3 or 5 defined by BARC (Bleeding Academic Research Consortium) criteria

  3. BARC type 2 ,3 or 5 bleeding events

    Time frame: 1, 6 and 12 months

    Bleeding events type 2, 3 or 5 defined by BARC (Bleeding Academic Research Consortium) criteria

  4. BARC defined type 2 bleeding events

    Time frame: 1, 6 and 12 months

    Bleeding events type 2 defined by BARC (Bleeding Academic Research Consortium) criteria

  5. Rate of NACE

    Time frame: 1 and 6 months

    NACE is a composite clinical endpoint of all-cause death, any stroke, any MI, any revascularization and BARC type 3 or 5 bleeding events

  6. Device-oriented Composite Endpoint (DoCE)

    Time frame: 1, 6 and 12 months

    DoCE is a composite clinical endpoint of cardiac cause death, target vessel myocardial infraction (TV-MI), and Clinically individual target lesion revascularization (CI-TLR)

  7. Cardiac death

    Time frame: 1, 6 and 12 months

    Rates of individual components of DoCE

  8. Target vessel myocardial infraction (TV-MI)

    Time frame: 1, 6 and 12 months

    Rates of individual components of DoCE

  9. Clinically individual target lesion revascularization (CI-TLR)

    Time frame: 1, 6 and 12 months

    Rates of individual components of DoCE

  10. Patient-oriented Composite Endpoint (PoCE)

    Time frame: 1, 6 and 12 months

    The primary safety endpoint of PoCE is defined as all-cause death, any stroke, any MI, any revascularization

  11. All-cause death

    Time frame: 1, 6 and 12 months

    Rates of individual components of PoCE

  12. Any MI

    Time frame: 1, 6 and 12 months

    Rates of individual components of PoCE

  13. Any stroke

    Time frame: 1, 6 and 12 months

    Rates of individual components of PoCE

  14. Any revascularization

    Time frame: 1, 6 and 12 months

    Rates of individual components of PoCE

  15. Target vessel failure (TVF)

    Time frame: 1, 6 and 12 months

    Target vessel failure is defined as cardiovascular death, target vessel myocardial infraction (TV-MI), and clinically-indicated target vessel revascularization

  16. Clinically-indicated target vessel revascularization

    Time frame: 1, 6 and 12 months

    Rates of individual components of TVF

  17. Definite/Probable stent thrombosis rates

    Time frame: 1, 6 and 12 months

Sponsors and collaborators

Lead sponsor

Xijing Hospital

Other

Registry information

Official study title

Aspirin Plus Ticagrelor for 1 Month Followed by 5 Months Ticagrelor Monotherapy Versus Aspirin Plus Ticagrelor for 12 Months in Acute Coronary Syndrome Patients With Drug-coated Balloon: a Multicentre, Randomized, Non-inferiority Trial

Acronym: CAGEFREEII

Important dates

Study start
2021
Primary completion
2024
Study completion
2026
First posted
Jul 21, 2021
Registry last updated
Nov 14, 2023

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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