Autopsy report · NCT06590571
The Study for Evaluate of Satety and Dfficacy of Hemostatic Device
Cause of deathDrug or device supply
“The company stopped manufacturing the product”
Life of this trial
- Registered 5 years 8 months after it had already started.
- Ran for about 3 years 1 month before it stopped.
- 227 participants enrolled.
- No results are posted on the registry.
Vital statistics
- Status
- Terminated
- Phase
- Na
- Sponsor
- Pusan National University Yangsan Hospital
- Sponsor type
- University, hospital or other
- Conditions
- Coronary Artery Disease
- Interventions
- TRAcelet™; Gauze pad
- Participants
- 227
- Sites
- 1
- Countries
- South Korea
Trials that died the same way
- Active Surveillance Post-Approval Atudy of the Stelkast Surpass Acetabular System
“Product is no longer being manufactured and marketed.” - A Pilot, Dose Escalating Study on VLX103 in Moderate Alcoholic Steatohepatitis
“Drug manufacturer ceased operations” - Oblimersen Sodium & Combination Chemotherapy in Treating Patients With Newly Diagnosed Diffuse Large B-Cell Lymphoma
“Manufacturer is no longer making the drug.” - Safety and Pharmacokinetics of UV-4B Solution Administered Orally as Multiple Ascending Doses to Healthy Subjects
“Product development halted for business reasons.” - Radiographic Analysis Using PureGen Versus Autologous Bone in Posterolateral Fusion (PLF)
“Product no longer on the market”
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.