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NCT Number: NCT06676553

INtraprocedural Feedback-Optimized Renal Denervation Based on Measurements Obtained Through Renal Artery Stimulation: a Randomized Controlled Trial (INFORM)

Our previous study (Huang HC, Pan HY, Wang TD, Circ Cardiovasc Interv 2023;16:e012779) demonstrated that when renal artery stimulation continues to trigger systolic blood pressure increases (>=20 mmHg increase compared to baseline) after the initial procedure, patients show poor blood pressure reduction 6 months following renal denervation. Based on this finding, we designed a proof-of-concept trial comparing two approaches: a guided strategy versus conventional renal denervation. In the guided strategy, we perform additional ablations of main and/or branch renal arteries if immediate post-procedure stimulation still elevates systolic blood pressure (>=20 mmHg increase compared to baseline). The conventional approach involves no repeat procedures. This trial aims to determine whether the guided strategy leads to better clinical outcomes, measured by 6-month ambulatory blood pressure changes, and to establish the value of using intraprocedural feedback to assess and guide renal denervation treatment.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

National Taiwan University Hospital

Taipei, 100225, Taiwan

Location status: Recruiting

Location contact

Tzung-Dau Wang, MD, PhD

CONTACT

[email protected]

886-972651070

Tzung-Dau Wang, MD, PhD

PRINCIPAL_INVESTIGATOR

About this study

  • Anesthesia: Intravenous propofol to achieve adequate sedation throughout the course.
  • Renal artery stimulation (RAS) will be performed at 2 sites (proximal and distal main renal artery) in both renal arteries. Pacing frequency was set at 10 Hz, pacing output at 20 mA with a pulse duration of 10 ms, and duration of 60 sec based on earlier researches. The maximal systolic blood pressure rise and branch renal artery constriction since the start of RAS till 3 minutes after its discontinuation will be recorded. The body reaction during RAS will be recorded (0, no response; 1, mild (voice) response; 2. limited movement; 3. significant movement).
  • Renal denervation (RDN) will be performed using the multielectrode Symplicity Spyral RDN catheter. The multielectrode RDN catheter contains 4 electrodes separated from each other in a spiral configuration. Up to 4 discrete radiofrequency (RF) ablations were applied simultaneously. Each application lasts ≤60 s with a power ≤8 Watts (W) and a target temperature of ≤70°C (158°F). Electrodes that do not reach the therapeutic temperature or impedance drop are automatically switched off.
  • Post RDN renal artery stimulation:

After RDN completed, renal artery stimulation will be repeated immediately. The maximal RAS-induced SBP changes will be recorded. All BP readings are the average of 8 consecutive beats by default (Siemens, Germany), which could minimize the inadvertent BP fluctuations by movements and respiration (8 beats could encompass at least one respiratory cycle). The branch renal artery constriction since the start of RAS till 3 minutes after its discontinuation will be recorded. The body reaction during RAS will be recorded (0, no response; 1, mild (voice) response; 2. limited movement; 3. significant movement).

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Patients with hypertension and are willing to undergo renal denervation.
  • Patients are treated with antihypertensive medications, or with an office systolic blood pressure (SBP) >140 mm Hg or diastolic blood pressure (DBP) >90 mm Hg, and 24-hour SBP of >130 mmHg or DBP >80 mm Hg, irrespective of antihypertensive treatment.

Exclusion criteria

  • An unsuitable renal artery anatomy for renal denervation, assessed by computed tomographic angiography (main renal artery lumen diameter <3 mm or a total length <20 mm).
  • Secondary hypertension, including hyperaldosteronism, pheochromocytoma, and renal artery stenosis (>50% stenosis in one or both arteries).

Treatment and study plan

Radiofrequency ablation alone, re-denervation to main and/or branch renal artery

Device

Re-denervation according to the site where renal artery stimulation can induce systolic blood pressure rise of >= 20 mmHg. Main renal artery denervation if proximal main renal artery stimulation positive, while branch renal artery denervation if distal main renal artery stimulation positive.

Radiofrequency ablation alone, no further renal denervation

Procedure

No further renal denervation after standard renal denervation even renal artery stimulation-induced systolic blood pressure rise >= 20 mmHg

Primary outcomes

  1. 24-hour systolic blood pressure reduction (compared to baseline)

    Time frame: 6 months following the index renal denervation

Secondary outcomes

  1. 24-hour diastolic blood pressure reduction (compared to baseline)

    Time frame: 6 months following the index renal denervation

  2. Awake and asleep systolic/diastolic blood pressure and heart rate changes (compared to baseline)

    Time frame: 6 months following the index renal denervation

  3. Serum creatinine and estimated glomerular filtration rate changes

    Time frame: 6 months following the index renal denervation

Other outcomes

  1. 24-hour blood pressure changes based on branch artery constriction following renal artery stimulation

    Time frame: 6 months following the index renal denervation

  2. 24-hour blood pressure reduction (compared to baseline)

    Time frame: 1 year and 2 years following the index renal denervation

Study contacts

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

Tzung-Dau Wang, MD, PhD

CONTACT

[email protected]

886-972651070

Ya-Chun Chen, BS

CONTACT

[email protected]

886-2-23123456 ext. 265877

Sponsors and collaborators

Lead sponsor

National Taiwan University Hospital

Other

Collaborators

  • Medtronic
  • Smart Health Technology Research and Development Center, National Taiwan University

Registry information

Official study title

INtraprocedural Feedback-Optimized Renal Denervation Based on Measurements Obtained Through Renal Artery Stimulation: a Randomized Controlled Proof-of-concept Trial to Assess Whether Renal Denervation Guided by Renal Artery Stimulation Outperforms Conventional Renal Denervation in 6-month Ambulatory Blood Pressure Reductions

Acronym: INFORM

Important dates

Study start
2024
Primary completion
2026
Study completion
2028
First posted
Nov 6, 2024
Registry last updated
Nov 6, 2024

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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