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Clinical Trial ● Currently Recruiting Non-phase study NCT06059638

BradycArdia paCemaKer With AV Interval Modulation for Blood prEssure treAtmenT

BradycArdia paCemaKer With AV Interval Modulation for Blood prEssure treAtmenT — Recruiting • Non-phase study • Cardiology / Cardiovascular • NCT06059638.

📅 17 Apr 2026 ⏱ 1 min read
Currently Recruiting
This trial is actively seeking participants in the UK. Discuss eligibility with your patient before referring.
Status
Currently Recruiting
Phase
Non-phase study
NCT ID
NCT06059638
Sponsor
Orchestra BioMed, Inc
Start
2023-12-27
ClinicaliQ Trial Snapshot
  • BradycArdia paCemaKer With AV Interval Modulation for Blood prEssure treAtmenT — Recruiting • Non-phase study • Cardiology / Cardiovascular • NCT06059638.
  • What is being tested: A novel atrioventricular interval modulation (AVIM) algorithm integrated into dual-chamber pacemakers to evaluate its safety and effectiveness as a potential blood pressure treatment strategy.
  • Patient eligibility overview: The trial includes patients requiring dual-chamber pacemaker implantation across multiple countries in a prospective, randomized, double-blind design, with specific eligibility criteria related to cardiac and blood pressure status (detailed criteria not specified in summary).
Use This Page For
  • Quick orientation before opening the registry record.
  • Checking recruitment status, phase and sponsor at a glance.
  • Connecting this trial to nearby guidelines, Drug Science and education.
What This Trial Is Studying

A prospective, multinational, randomized, double-blind, clinical trial evaluating the safety and effectiveness of a novel atrioventricular interval modulation (AVIM) algorithm downloaded into a dual-chamber Medtronic Astra/Azure pacemaker.

Eligibility Snapshot
  • :
  • Patient has or is indicated for a dual-chamber pacemaker. Visit 1 can be performed within 30 days prior to a planned implant of a Medtronic Astra/Azure dual-chamber pacemaker system or at any time thereafter 2. On a stable antihypertension treatment regimen with at least 1 class of antihypertensive drug 3. Office SBP ≥135 mmHg and

Use the source registry for the full inclusion and exclusion criteria before discussing referral or enrolment.

Full Trial Details
View this trial on the source registry
Eligibility criteria, protocol, and results when available
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