Autopsy report · NCT03300167
Study of the Vascular Response to Percutaneous Coronary Intervention in Patients With Non-ST-elevation Acute Coronary Syndromes Using Intravascular Blood Sampling
Cause of deathStaffing, sites or logistics
“Delivery of equipment. PI not had any further interaction with the company so closed 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- Withdrawn before it enrolled anyone.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- Withdrawn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
- Na
- Sponsor
- Sheffield Teaching Hospitals NHS Foundation Trust
- Sponsor type
- University, hospital or other
- Conditions
- Non ST Segment Elevation Acute Coronary Syndrome
- Interventions
- The Liquid Biopsy System
- Participants
- 0
- Sites
- 1
- Countries
- United Kingdom
Trials that died the same way
- Noninvasive Cardiac Output Measurements in Patients With Pulmonary Hypertension Undergoing Right Heart Catheterization With Acute Vasodilator Testing
“The PI closed this study and went to another institution.” - Electrode Placement and Audiologic Outcomes With the Advanced Bionics HiFocus L23 Electrode
“device under study complication-due to PI departure, study closed and will not reopen” - 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.” - Pre-post Spinal Popliteal Block
“Retrospective study that the PI decided not to proceed with” - Pimavanserin for Sleep in Parkinson Disease
“The PI did not have eligible candidates. Therefore, Acadia Pharmaceuticals (the sponsor) closed the study.”
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.