Autopsy report · NCT01943565
Intrathecal Hydromorphone for Post-cesarean Delivery Pain - a Dose Finding Study
Cause of deathOther
“Research question answered by another group of researchers (Sviggum et al)”
Life of this trial
- Registered 1 year 3 months before it started.
- Ran for about 1 year 8 months before it stopped.
- 29 participants enrolled.
- Results were posted on the registry 10 months after it ended.
Vital statistics
- Status
- Terminated
- Phase
- Phase 4
- Sponsor
- Brigham and Women's Hospital
- Sponsor type
- University, hospital or other
- Conditions
- Healthy; Pain; Pregnancy
- Interventions
- Hydromorphone 25mcg; Hydromorphone 50mcg; Hydromorphone 100mcg; spinal anesthesia
- Participants
- 29
- Sites
- 1
- Countries
- United States
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.