Autopsy report · NCT02603549
Pituitary Function and Spontaneous Intracranial Hypotension
Cause of deathRegulatory or ethics
“Study protocol needs to be amended. Recruitment is halted until amendment is completed and approved by IRB.”
Life of this trial
- Registered 4 months after it had already started.
- Suspended: paused, and may or may not restart.
- 100 participants planned (an estimate, not an actual count).
Vital statistics
- Status
- Suspended
- Sponsor
- Cedars-Sinai Medical Center
- Sponsor type
- University, hospital or other
- Conditions
- Hyperprolactinemia; Spontaneous Intracranial Hypotension
- Interventions
- Pituitary panel will be drawn pre-op and post-op for all patients.
- Participants
- 100 (planned, not actual)
- Sites
- 1
- Countries
- United States
Trials that died the same way
- Study of ASN-002 to Treat Basal Cell Carcinomas (BCCs) in Individuals With Basal Cell Nevus Syndrome (BCNS)
“Study did not start. Another protocol is being developed. Recruitment on hold.” - Clinical Data Collection for Obstetric Ultrasound Algorithms
“Study paused temporarily pending IRB approval of an amendment to the protocol and consent form.” - Timing of VTE Prophylaxis in TBI
“Recruitment not started due to potential conflicting study at same institution. May renew study in the future.” - Clonidine for Neonatal Abstinence Syndrome Study
“Based on the planned interim analysis results at 50% recruitment, after IRB reviewed the results, further enrollment was stopped.” - Methadone as an Alternative Treatment for Children Underdoing HSCT
“Study is closed with the IRB due to no funding. May resume once funding is obtained.”
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.