Autopsy report · NCT03101098
Retroperitoneal Ligation of Uterine Artery in Total Laparoscopic Hysterectomy for Enlarged Uterus
Cause of deathRegulatory or ethics
“IRB did not approve this study.”
Life of this trial
- Suspended: paused, and may or may not restart.
- 54 participants planned (an estimate, not an actual count).
Vital statistics
- Status
- Suspended
- Phase
- Na
- Sponsor
- Kangbuk Samsung Hospital
- Sponsor type
- University, hospital or other
- Conditions
- Hysterectomy
- Interventions
- Retroperitoneal liagation of uterine artery; Classical ligation of uterine artery
- Participants
- 54 (planned, not actual)
- Sites
- 1
- Countries
- South Korea
Trials that died the same way
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“Study did not receive IRB approval.” - Light Therapy to Treat Depression in Pediatric Stem Cell Therapy Recipients
“The study did not enroll participants and had not shown significant progress since the initial IRB approval.” - Study Comparing Intubation Via Video Laryngeal Mask Airways (VLMAs) Versus Video Laryngoscopy
“Study never approved by the IRB. Was not initiated” - Rituximab, Venetoclax, and Bortezomib for the Treatment of Relapsed or Refractory Diffuse Large B-Cell Lymphoma
“This study was never submitted to the IRB for review and approval. No research subjects were enrolled. .” - Antibiotics and Tissue Expanders in Breast Reconstruction
“The study was withdrawn prior to IRB approval.”
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.