Autopsy report · NCT05354791
Pre-post Spinal Popliteal Block
Cause of deathFunding or business, also staffing, sites or logistics
“Retrospective study that the PI decided not to proceed with”
Life of this trial
- Registered 11 months after it had already started.
- Ran for about 1 year 10 months before it stopped.
- 1,500 participants enrolled.
- No results are posted on the registry.
Vital statistics
- Status
- Terminated
- Sponsor
- Hospital for Special Surgery, New York
- Sponsor type
- University, hospital or other
- Conditions
- Foot Surgery; Ankle Surgery
- Participants
- 1,500
- Sites
- 1
- Countries
- United States
Trials that died the same way
- Pilot Study Investigating the Use of the ReBuilder to Treat Chemotherapy Induced Peripheral Neuropathy in Patients With Breast Cancer
“PI decided no longer to pursue” - Optimal A1c Control in Post Liver or Combined Liver and Kidney Transplant Recipients Who Have Diabetes Mellitus
“PI decided to stop the study” - Study of the Anti-PD-1 Antibody Nivolumab in Combination With Dabrafenib and/or Trametinib
“PI decided not to proceed” - Affective Processing in Depression and Epilepsy
“PI wanted to discontinue study.” - Carry-over Effects of Repetitively Applied Transcutaneous Spinal Cord Stimulation on Spasticity
“Study terminated by the PIs due to unexpected outcomes”
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.