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NCT06036186Completed

Study for the Treatment of Heart Failure With Preserved Ejection Fraction Associated With High Blood Pressure Using Right Atrial Pacing Controlled by the PressurePaceTM System

Early Feasibility, Randomized Crossover and Double-Blind Design, Study for the Treatment of Heart Failure With Preserved Ejection Fraction (HFpEF) Associated With Hypertension Utilizing Right Atrial Pacing Regulated by the PressurePace™ System (RelieveHFpEF-II)

Source: ClinicalTrials.gov · Last updated 17 May 2024

Brief summary (registry, in English)

This study is a prospective, double blind, self-controlled, randomized, cross-over study to evaluate the feasibility, efficacy, and safety of treating patients with Heart Failure with preserved Ejection Fraction (HFpEF) associated with hypertension using the PressurePace™ system of Right Atrial Pacing regulated by blood pressure in subjects with dual chamber pacemakers. The objective of this study is to show that blood pressure-controlled right atrial pacing improves exercise tolerance, improves heart failure symptoms, and improves hypertension control in subjects with HFpEF associated with hypertension compared to conventional bradycardia pacing alone.

Status (registry)
Completed
Study type
Interventional
Enrollment
16 (actual)
First submitted
16 Aug 2023
Start date
26 Aug 2023
Primary completion date
12 Apr 2024
Lead sponsor
BaroPace Inc.
NCT number
NCT06036186

What you commit to

  • Study type: Interventional
  • Participants enrolled: 16
  • From 26 Aug 2023 to the primary completion date, 12 Apr 2024
  • 3 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Indications for emergency surgery at time of screening or planned surgery before the 49-day follow-up
  • Hospitalized in the prior six months for a heart attack, stroke, or TIA, or have a history of blood-pressure related syncope in last 6 months.

Other illness

  • Physical or psychological condition which would impair study participation.
  • End Stage Renal Disease on haemodialysis
  • Prone to atrial or ventricular arrhythmias with altered pacing.
  • Unstable from a cardiovascular standpoint, such as on-going chest pain, the diagnosis of heart failure with reduced EF, or who report being ill or otherwise uncomfortable, medically, or psychologically at the time of study.

Other

  • A resting SBP \> 170 mmHg, or \< 130 SBP at screening average over 3 readings in 30 minutes. The readings will be taken with the blood pressure cuff on the subject's left arm while seated after at least ten minutes of rest. Consecutive readings will be taken at least 10 minutes apart.
  • A resting DBP \> 120 mmHg, or \< 80 at screening average over 3 measurements in 30 minutes.
  • Pregnant or breast-feeding.
  • Have a pacemaker that is currently the subject of a manufacturer's recall or regulatory advisory of malfunction.
  • Unable to interact and execute commands with the BaroPace modules during the screening phase.
  • Taking short acting Nifedipine or Clonidine or taking ISA Beta Blockers; Acebutolol, Pindolol, Sectral or Visken

Who the study is looking for

  • Have a Pacetronix dual chamber pacemaker implanted for \> 2 weeks that is more than 6 months from ERI (elective replacement indicator).
  • Ages: Adult subjects \> 35 years and \< 90 of age.
  • Have heart failure with preserved ejection fraction defined as ejection fraction \> 45 percent.
  • Have hypertension (SBP \>135 mmHg) within 30 days before the start of screening, despite at least one or more medication for the treatment of hypertension.
  • Screening average right atrial pacing \< 50% and average intrinsic/pacing heart rate \< 70 bpm over the previous clinical monitoring period of the pacemaker diagnostics of at least 14 days
  • Blood pressure of no less than 135 systolic and a diastolic blood pressure no less than 85 mm Hg at initial screening over 3 readings in 30 minutes in the sitting position, in the left arm.
  • Able to tolerate at least 3 minutes of a Modified Bruce Protocol Treadmill
  • Physically capable and willing to perform repeated 6-minute walk tests associated with the study, and a baseline distance of at least 225 meters. Symptoms limiting the duration of the 6-minute walk test must be due to heart failure alone.
  • Willing and able to sign consent.
  • Stable medications for Hypertension for at least 4 weeks prior to screening.

Age in the registry: 35 years to 90 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (3)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Dr. C. M. Chopra Hospital & Heart Care Centre
Coordinator of this site? Confirm its status
JaipurIndiaUnknown status
Maharaja Agrasen Superspeciality Hospital, Clinical Research Department, Basement, Main Building, Room No-09, Sector-07, Agrasen Aspatal Marg, Central Spine, Vidyadhar Nagar,
Coordinator of this site? Confirm its status
JaipurIndiaUnknown status
L.P.S. Institute of Cardiology, G.S.V.M Medical College
Coordinator of this site? Confirm its status
KanpurIndiaUnknown status

Related publications

This page is information, not medical advice. Discuss any trial with your doctor.