Autopsy report · NCT04008043
Pilot Study: Effect of Dexamethasone vs Vicodin in Reducing Post-operative Pain
Cause of deathStaffing, sites or logistics
“Inadequate resources to start the study at this site.”
Life of this trial
- Withdrawn before it enrolled anyone. Its dates are the sponsor's plans, not events that happened.
Vital statistics
- Status
- Withdrawn
- Phase
- Phase 4
- Sponsor
- Boston University
- Sponsor type
- University, hospital or other
- Conditions
- Oral Surgery
- Interventions
- Vicodin; Dexamethasone
- Participants
- 0
- Sites
- 1
- Countries
- United States
Trials that died the same way
- Comparison of da Vinci Simulator vs LapSim Simulator
“Not enough resources to start the study” - HBOT Late Radiation Tissue Injury
“Lack of resources to complete the study” - Mindfulness in Medical Training
“Not enough resources to proceed with the study” - Noninvasive NAVA Versus NIPPV in Low Birthweight Premature Infants
“Insufficient resources available to complete the study” - Home-based SSP on Individuals With PWS
“Insufficient resources to complete study as planned”
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.