Autopsy report · NCT02195310
The Use of PrevenaTM on Clean Closed Sternal Midline Incisions in Subjects at High Risk for Surgical Site Occurrences.
Cause of deathFutility
“due to futility”
Life of this trial
- Registered 8 months after it had already started.
- Ran for about 2 years 11 months before it stopped.
- 342 participants enrolled.
- Results were posted on the registry 2 years 10 months after it ended.
Vital statistics
- Status
- Terminated
- Phase
- Na
- Sponsor
- Solventum US LLC
- Sponsor type
- Industry
- Conditions
- Surgical Site Occurences After Sternotomy; Wound Infection
- Interventions
- Prevena™ Incision Management System; Conventional sterile wound dressings
- Participants
- 342
- Sites
- 13
- Countries
- Austria, Germany, Netherlands
Trials that died the same way
- Radiation Post-CAR T in Refractory Lymphoma
“Futility” - Safety of FMT: OpenBiome Outcomes and Longitudinal Follow-up (STOOL) for Recurrent Clostridium Difficile Infection
“for futility” - Prevention of Unexplained Recurrent Abortion by Enoxaparine
“Stopped for futility” - The Effectiveness of Non-Pyrethroid Insecticide-Treated Durable Wall Liners as a Method for Malaria Control in Endemic Rural Tanzania
“futility ground” - Safety and Efficacy Study of AVB-S6-500 (Batiraxcept) in Patients With Advanced or Metastatic Clear Cell Renal Cell Carcinoma
“Due to business reasons”
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.