Autopsy report · NCT03613090
Novel Collagen Scaffold vs Conventional Scaffold in Regeneration of Human Dental Pulp Tissue
Cause of deathRegulatory or ethics
“Withdrawn-was not approved by IRB”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- Withdrawn before it enrolled anyone.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- Withdrawn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 2
- Sponsor
- University of Alabama at Birmingham
- Sponsor type
- University, hospital or other
- Conditions
- Root Canal Therapy
- Interventions
- Collagen-hydroxyapatite scaffold (Syn-Oss); Collagen Scaffold (Colla-Plug)
- Participants
- 0
- Sites
- 1
- Countries
- United States
Trials that died the same way
- Impact of Cardiac Resynchronization Therapy on Right Ventricular Function in Left Ventricular Assist Device Patients
“IRB Approval withdrawn” - Feasibility of Ultra-sound Guided Radiofrequency Ablation in the Management of Head and Neck Neoplasia.
“Administratively withdrawn by the IRB prior to IRB approval” - Prospective Trial of Alerting to Extended Hypotensive Exposures on Long-Term Outcome After Surgery
“IRB application withdrawn” - Low-Level Transcutaneous Vagus Stimulation in ST Segment Elevation Myocardial Infarction: TREAT MI Study
“Study never initiated; withdrawn prior to receiving IRB approval” - Antibiotics and Tissue Expanders in Breast Reconstruction
“The study was withdrawn prior to IRB approval.”
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.