Autopsy report · NCT06638749
Effect of TXA on Blood Loss in Reverse Total Shoulder Arthroplasty
Cause of deathRegulatory or ethics
“Administrative withdrawal-study not approved by 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- Withdrawn before it enrolled anyone.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- Withdrawn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
- University of Kansas Medical Center
- Sponsor type
- University, hospital or other
- Conditions
- Shoulder Arthritis; Blood Loss, Surgical; Tranexamic Acid Adverse Reaction
- Interventions
- Tranexamic Acid; Normal Saline
- Participants
- 0
- Sites
- 1
- Countries
- United States
Trials that died the same way
- Low-Level Transcutaneous Vagus Stimulation in ST Segment Elevation Myocardial Infarction: TREAT MI Study
“Study never initiated; withdrawn prior to receiving IRB approval” - Antibiotics and Tissue Expanders in Breast Reconstruction
“The study was withdrawn prior to IRB approval.” - Novel Collagen Scaffold vs Conventional Scaffold in Regeneration of Human Dental Pulp Tissue
“Withdrawn-was not approved by IRB” - A Prospective Randomized Comparison of Three Methods for Fixation of Hammertoes
“Study withdrawn from IRB approval process by PI” - Suprainguinal Fascia Iliaca Compartment Block in Direct Anterior Approach to Total Hip Arthroplasty
“Study never approved by IRB or initiated”
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.