Autopsy report · NCT00334685
[S,S]-Reboxetine Add-On Trial
Cause of deathFutility
“The Data Monitoring Committee terminated the study on the basis of futility (insufficient clinical response).”
Life of this trial
- Registered 2 months before it started.
- Ran for about 1 year 2 months before it stopped.
- 136 participants enrolled.
- No results are posted on the registry.
Vital statistics
- Status
- Terminated
- Phase
- Phase 2
- Sponsor
- Pfizer
- Sponsor type
- Industry
- Conditions
- Pain
- Interventions
- [S,S]-Reboxetine + Pregabalin; Pregabalin
- Participants
- 136
- Sites
- 83
- Countries
- Austria, Canada, Czechia, Germany, Italy, Latvia, Netherlands, Norway, Poland, Russia, Spain, Sweden and more
Trials that died the same way
- Minocycline for the Treatment of Decreased Mental Function in HIV-Infected Adults
“This study was terminated early due to futility.” - Removal Versus Retention of Cerclage in Preterm Premature Rupture of Membranes (PPROM)
“This trial was terminated following a futility analysis confirming futility of continuing the study” - Trial to Evaluate UltraSound in the Treatment of Tibial Fractures
“Study was terminated due to futility” - CONvalescent Plasma for Hospitalized Adults With COVID-19 Respiratory Illness (CONCOR-1)
“Study was terminated after the planned interim analysis as the pre-defined futility threshold was met” - Study of Nintedanib and Chemotherapy for Advanced Pancreatic Cancer
“The study was terminated due to futility and lack of future funding”
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.