Rate Control in Patients With Atrial Fibrillation
RaP-AF
The Surrogate Marker of Rate Control in Patients With Atrial Fibrillation
1 other identifier
interventional
13
1 country
1
Brief Summary
To search for the best marker for the patients in atrial fibrillation with rate control
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable atrial-fibrillation
Started Oct 2020
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
August 9, 2020
CompletedFirst Posted
Study publicly available on registry
August 14, 2020
CompletedStudy Start
First participant enrolled
October 21, 2020
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 21, 2022
CompletedStudy Completion
Last participant's last visit for all outcomes
July 1, 2022
CompletedJanuary 16, 2026
January 1, 2026
1.7 years
August 9, 2020
January 15, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Change of Maximal Oxygen consumption
acquire the data by Cardiopulmonary exercise test (CPET) with different (low and high) drug dosages for rate control
0, 3, 6 months
Study Arms (1)
rate control
EXPERIMENTALInterventions
Start with empirical lower dose for 3 months, and then titrate up
Eligibility Criteria
You may qualify if:
- \~90 years old
- Rate control is preferred after shared decision making
You may not qualify if:
- cannot cooperate with or complete CPET
- has contraindication for CPET, such as uncontrolled heart failure, hypertension, angina, valvular heart disease, lung function impariment that SaO2\<90% at room air.
- Ventricular rate below 80/min before any medication
- Permanent pacemaker implanted
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
National Taiwan University Hospital
Taipei, Taiwan
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Chih-Chieh Yu, MD.PhD
National Taiwan University Hospital
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- SEQUENTIAL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
August 9, 2020
First Posted
August 14, 2020
Study Start
October 21, 2020
Primary Completion
June 21, 2022
Study Completion
July 1, 2022
Last Updated
January 16, 2026
Record last verified: 2026-01