Autopsy report · NCT03871751
Home-based SSP on Individuals With PWS
Cause of deathStaffing, sites or logistics
“Insufficient resources to complete study as planned”
Life of this trial
- Registered 1 month before it started.
- Ran for about 8 months before it stopped.
- 10 participants enrolled.
- No results are posted on the registry.
Vital statistics
- Status
- Terminated
- Phase
- Na
- Sponsor
- Indiana University
- Sponsor type
- University, hospital or other
- Conditions
- Prader-Willi Syndrome
- Interventions
- Safe and Sound Protocol
- Participants
- 10
- Sites
- 1
- Countries
- United States
Trials that died the same way
- Noninvasive NAVA Versus NIPPV in Low Birthweight Premature Infants
“Insufficient resources available to complete the study” - HBOT Late Radiation Tissue Injury
“Lack of resources to complete the study” - RescueTEE for In-hospital Cardiac Arrest (ReTEECA Trial)
“Not enough resources to execute study” - Comparison of da Vinci Simulator vs LapSim Simulator
“Not enough resources to start the study” - Mindfulness in Medical Training
“Not enough resources to proceed with the 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.