Autopsy report · NCT02710669
New Formulations of Propafenone to Treat Atrial Fibrillation
Cause of deathStaffing, sites or logistics
“Study halted/terminated prematurely due to COVID.”
Life of this trial
- Registered 7 months before it started.
- Ran for about 3 years 6 months before it stopped.
- 193 participants enrolled.
- Results were posted on the registry 1 year 1 month after it ended.
Vital statistics
- Status
- Terminated
- Phase
- Phase 1, Phase 2
- Sponsor
- Vanderbilt University
- Sponsor type
- University, hospital or other
- Conditions
- Atrial Fibrillation
- Interventions
- (R)-propafenone; (S)-Propafenone; Placebo
- Participants
- 193
- Sites
- 1
- Countries
- United States
Trials that died the same way
- Effects of E-Cigarette Power and Nicotine Content in Dual Users and Vapers
“Study terminated due to COVID” - Effects of Community-center Based Dietary Intervention on Frailty Prevention and Regression in the Elderly.
“Due to the impacts of COVID-19, the study had to terminate.” - Comparison of Efficacy of Behavioral Approaches for Treatment of Insomnia
“Study halted prematurely and will not resume; participants are no longer being examined or receiving intervention. COVID Complications.” - Acceptability, Feasibility and Safety of a Yoga Program for Chronic Pain in Sickle Cell Disease
“Study terminated due to COVID-19 pandemic.” - RAman For Thyroid cancER
“Covid19 halted study”
Look deeper
- The official registry record (the source of truth)
- Record history: every change the sponsor made
- Open it in the database
Everything here comes from the current ClinicalTrials.gov record. The timeline uses the record’s dates; dates marked planned are the sponsor’s plans. The cause of death is an automatic, unverified label. This is research information, not medical advice.