Autopsy report · NCT05724628
Non-operative vs. Operative Management of Acute Appendicitis in Vulnerable Patient Populations
Cause of deathRegulatory or ethics, also staffing, sites or logistics
“Project did not receive final IRB approvals. PI decided to withdrawn research study.”
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- Withdrawn before it enrolled anyone.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- Withdrawn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 1
- Sponsor
- University of Texas Southwestern Medical Center
- Sponsor type
- University, hospital or other
- Conditions
- Acute Appendicitis
- Interventions
- Laparoscopic appendectomy; Antibiotics (IV transitioned to oral)
- Participants
- 0
Trials that died the same way
- A Prospective Randomized Comparison of Three Methods for Fixation of Hammertoes
“Study withdrawn from IRB approval process by PI” - Real-time 3-Dimensional Echocardiography for Assessment of Cardiac Function and Congenital Heart Disease
“Study did not receive IRB approval.” - Sensory-Play Based (SenPlay) Intervention for Young Children With or At Risk for ADHD
“Study closed by the IRB when PI did not submit for annual review.” - Antibiotics and Tissue Expanders in Breast Reconstruction
“The study was withdrawn prior to IRB approval.” - Low-Level Transcutaneous Vagus Stimulation in ST Segment Elevation Myocardial Infarction: TREAT MI Study
“Study never initiated; withdrawn prior to receiving IRB approval”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.