Chloroquine for Patients With Symptomatic Persistent Atrial Fibrillation: A Prospective Pilot Study
Part of paid clinical trials in Tampa, Florida.
- Sponsor
- University of South Florida
- Study ID
- NCT02932007
- Phase
- PHASE2
- Status
- Recruiting
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Chloroquine Phosphate — DRUGTwo tablets of study drug are to be taken on the day of study drug initiation and the next day, followed by one tablet each day for the next 12 days. Study drug to be orally administered and taken with food.
Study Details
The goal of this pilot study is to explore the efficacy of chloroquine in terminating persistent AF and assess its potential role as a pharmacological cardioversion agent for the management of AF.
Key Dates
- Start date
- Mar 28, 2017
- Status verified
- Oct 2018
- Primary completion
- Mar 31, 2020
- Completion
- Sep 30, 2020
Study Design
- Enrollment
- 40 participants (estimated)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: Chloroquine PhosphateChloroquine Phosphate will be provided at 500 mg dosage strength for oral administration. Patient will be instructed to take 2 tablets per day on the first two days and 1 tablet each day for the next 12 days for a total of 14 days treatment.
Primary Outcome Measure
Proportion of patients with termination of AF [ Time Frame: Within 2 weeks of study drug initiation ]
Central Contacts
- Thanh Tran, MPH813-844-8544
- Sami Noujaim, PhD813-974-6416
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| University of South Florida | Tampa | Florida | 33606 | Jacob Siddoway Sami Noujaim, PhD (PRINCIPAL_INVESTIGATOR) Bengt Herweg, MD (SUB_INVESTIGATOR) Dany Sayad, MD (SUB_INVESTIGATOR) |
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