Autopsy report · NCT04011592
Efficacy And Tolerability Of Sub-Anesthetic Ketamine In Postpartum Depression
Cause of deathOther
“Recruitment not feasible”
Life of this trial
- Registered 4 months after it had already started.
- Ran for about 6 months before it stopped.
- 1 participant enrolled.
- Results were posted on the registry 1 year after it ended.
Vital statistics
- Status
- Terminated
- Phase
- Phase 2
- Sponsor
- The University of Texas Health Science Center, Houston
- Sponsor type
- University, hospital or other
- Conditions
- Post Partum Depression
- Interventions
- Ketamine 0.5 mg/kg; Ketamine 0.2 mg/kg
- Participants
- 1
- 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.