Autopsy report · NCT03925155
RCT Investigating Pre-cesarean Vaginal Wash of Chlorhexidine vs Povidone-iodine for Patient With Ruptured Amniotic Membrane.
Cause of deathRegulatory or ethics
“The study was withdrawn from the IRB”
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- Withdrawn before it enrolled anyone.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- Withdrawn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 3
- Sponsor
- Montefiore Medical Center
- Sponsor type
- University, hospital or other
- Conditions
- Cesarean Section Complications
- Interventions
- EZ scrub vaginal chlorhexidine 4% solution; 10% provodine-iodine vaginal preparation
- Participants
- 0
Trials that died the same way
- Antibiotics and Tissue Expanders in Breast Reconstruction
“The study was withdrawn prior to IRB approval.” - A Quality of Life Study Using Insulin Potentiation Targeted LowDose (IPTLD) Chemotherapy and Nutrition Therapy in the Treatment of Cancer
“The IRB which was overseeing the study stopped overseeing it” - Low-Level Transcutaneous Vagus Stimulation in ST Segment Elevation Myocardial Infarction: TREAT MI Study
“Study never initiated; withdrawn prior to receiving IRB approval” - Impact of Early Diagnosis and Treatment of OSA on Hospital Readmission in Hospitalized COPD Patients
“The study was withdrawn prior to initiation. The protocol was submitted for IRB review but was not approved. No participants were enrolled.” - CPAP Population Management
“The study was withdrawn prior to initiation. The protocol was submitted for IRB review but was not approved, and no participants were enrolled.”
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.