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NCT06445439 · ClinicalTrials.gov registry record · NA
Optimal Pacing Rate for Cardiac Resynchronization Therapy
A NA study of Atrial Fibrillation, Persistent, sponsored by Medstar Health Research Institute.
- Recruiting
- Registry status
- NA
- Development phase
- 60
- Enrollment target
- 5
- Study locations
NCT06445439 is a NA study of Atrial Fibrillation, Persistent that is actively recruiting participants, run by Medstar Health Research Institute. The registered enrollment target is 60 participants, below the 192-participant average among 3 other Atrial Fibrillation, Persistent trials with a reported enrollment target (69% lower). The trial reports 5 study locations across 3 states.
The verdict
NCT06445439, a NA study of Atrial Fibrillation, Persistent, is actively recruiting participants, sponsored by Medstar Health Research Institute.
- RECRUITING
- Registry status
- NA
- Development phase
- 60 participants
- Enrollment target
- 5
- Study locations
Study Summary
This is a prospective, randomized crossover study. The objective of the study is to determine if a pacing rate of 80 beats per minute (bpm) improves exercise tolerance during the 6-minute walk test. The investigators will randomly assign half of the participants to a starting rate of 60 bpm and then switch them to a rate of 80 bpm for 3 months, and vice versa.
Conditions Studied
Interventions
- DEVICE Pacing rate of 80 bpm
- DEVICE Pacing rate of 60 bpm
Study Locations (5)
District of Columbia
- MedStar Georgetown University Hospital - Washington D.C.
- MedStar Washington Hospital Center - Washington D.C.
Maryland
- MedStar Union Memorial Hospital - Baltimore
- MedStar Southern Maryland Hospital - Clinton
Virginia
- MedStar Heart and Vascular Office at Fairfax - Fairfax
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 60 participants |
| Start Date | 2023-12-19 |
| Est. Completion | 2025-08 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06445439
The ClinicalTrials.gov registry entry for NCT06445439 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 60 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 192-participant average among 3 other Atrial Fibrillation, Persistent trials with a reported enrollment target (69% lower). The listed sponsor is Medstar Health Research Institute, which has 115 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Atrial Fibrillation, Persistent appearing as the primary indexed condition, and to 2 interventions - of which Pacing rate of 80 bpm is the first listed.
NCT06445439 reports 5 study locations spanning 3 distinct geographic areas - top geographies include District of Columbia, Maryland, Virginia.
Frequently Asked Questions
What is clinical trial NCT06445439 about?
NCT06445439 is a clinical study titled "Optimal Pacing Rate for Cardiac Resynchronization Therapy". This is a prospective, randomized crossover study. The objective of the study is to determine if a pacing rate of 80 beats per minute (bpm) improves exercise tolerance during the 6-minute walk test. The investigators will randomly assign half of the participants to a starting rate of 60 bpm and then...
What is the current status of trial NCT06445439?
This trial is currently recruiting. It is a NA study. The enrollment target is 60 participants. The study started on 2023-12-19. Estimated completion is 2025-08.
What conditions does trial NCT06445439 study?
This clinical trial studies the following conditions: Atrial Fibrillation, Persistent.
What interventions are being tested in trial NCT06445439?
The interventions under investigation include: Pacing rate of 80 bpm (DEVICE), Pacing rate of 60 bpm (DEVICE).
Who is sponsoring clinical trial NCT06445439?
This trial is sponsored by Medstar Health Research Institute, which has 115 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06445439 being conducted?
This trial has 5 study locations across District of Columbia, Maryland, Virginia. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Related
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