Trial · NCT03987204
Ivabradine for Rate Control in Permanent Atrial Fibrillation
NCT03987204, Phase 1, Completed, Yale University
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Ivabradine for Rate Control in Permanent Atrial Fibrillation. Trials, record NCT03987204. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT03987204
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Ivabradine for Rate Control in Permanent Atrial Fibrillation
- NCT number
- NCT03987204
- Status
- Completed
- Phases
- Phase 1
- Enrollment
- 4 participants, actual
- Lead sponsor
- Yale University
- Conditions
- Atrial Fibrillation, Atrial Fibrillation, Persistent
- Interventions
- Ivabradine
- First posted
- 2019-06-14
- Last updated
- 2021-07-02
Source ClinicalTrials.gov
Registered outcomes5
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Heart Rate in Daily Life | 2 weeks | Average ventricular heart rate derived using pacemaker interrogation over 2 weeks |
| Primary | Percent Pacing in Daily Life | 2 weeks | Average percent pacing derived using pacemaker interrogation over 2 weeks |
| Primary | Heart Rate on Treadmill | 2 weeks | Average ventricular heart rate will be recorded after the patient exercises on a treadmill using a heart rate monitor |
| Primary | Symptoms and Exercise Tolerance | 2 weeks | Patients will undergo a 6 minute walk test, and symptoms and distance walked as measured by standard 6 minute walk protocol |
| Secondary | Blood Pressure | 2 weeks | Blood pressures will be monitored using a blood pressure cuff with the patient at rest for 10 minutes |
Source ClinicalTrials.gov
Outcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers0
The papers the trial lists on ClinicalTrials.gov.
None in this release.
Grants0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
None in this release.
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT03987204
GET https://conductscience.org/api/trials/v1/NCT03987204/registered