Autopsy report · NCT03284281
Low-Level Transcutaneous Vagus Stimulation in ST Segment Elevation Myocardial Infarction: TREAT MI Study
Cause of deathRegulatory or ethics
“Study never initiated; withdrawn prior to receiving IRB approval”
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- Withdrawn before it enrolled anyone.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- Withdrawn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
- Na
- Sponsor
- University of Oklahoma
- Sponsor type
- University, hospital or other
- Conditions
- STEMI - ST Elevation Myocardial Infarction; Inflammation
- Interventions
- Tragus stimulator; Sham Tragus stimulator
- Participants
- 0
- Sites
- 1
- Countries
- United States
Trials that died the same way
- Antibiotics and Tissue Expanders in Breast Reconstruction
“The study was withdrawn prior to IRB approval.” - Suprainguinal Fascia Iliaca Compartment Block in Direct Anterior Approach to Total Hip Arthroplasty
“Study never approved by IRB or initiated” - Study Comparing Intubation Via Video Laryngeal Mask Airways (VLMAs) Versus Video Laryngoscopy
“Study never approved by the IRB. Was not initiated” - Effect of TXA on Blood Loss in Reverse Total Shoulder Arthroplasty
“Administrative withdrawal-study not approved by IRB” - Simvastatin Nasal Rinses for the Treatment of COVID-19 Mediated Dysomsia
“Study halted prematurely; IRB approval not 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.