Autopsy report · NCT04254809

Evaluation of a Computerized Intervention for Learning to Re-Evaluate Suicidal Thoughts

“Face-to-face appointments, which were required by the IRB for suicide risk evaluation, were suspended by the IRB during the COVID-19 pandemic. During this pause, the PI left the institution. Thus, all study activities were terminated.”

The sponsor’s own words in the registry.

Life of this trial

• Registered 1 year 4 months after it had already started.
• Ran for about 1 year 10 months before it stopped.
• 96 participants enrolled.
• Results were posted on the registry 1 year 4 months after it ended.

Vital statistics

Status

Terminated

Phase

Na

Sponsor

Florida State University

Sponsor type

University, hospital or other

Conditions

Suicidal Ideation

Interventions

Re-Evaluating Suicidal Thoughts; Healthy Social Living

Participants

96

Sites

1

Countries

United States

Trials that died the same way

• Dietary Protein and Monocyte/Macrophage Mammalian Target of Rapamycin (mTOR) Signaling
  “Temporarily paused due to COVID-19 and expected to resume. This is not a suspension of IRB approval. PI has left the institution.” (73% match in meaning)
• Bortezomib in Combination With Ibrutinib in Ibrutinib Relapsed Mantle Cell Lymphoma
  “Enrollment and/or interactions/interventions temporarily paused due to COVID-19 and expected to resume in the future. This is not a suspension of IRB approval.” (69% match in meaning)
• A Pragmatic Randomized Trial of Icosapent Ethyl for High-Cardiovascular Risk Adults
  “The study was suspended by the IRB of record and subsequently terminated” (67% match in meaning)
• The Role of Hepatic Denervation in the Dysregulation of Glucose Metabolism in Liver Transplant Recipients
  “Permanently terminated due to COVID-19 given the poor vaccine penetrance in liver transplant recipients. This is not a suspension of IRB approval.” (66% match in meaning)
• Adherence to Otezla
  “Terminated IRB approval 6/26/2024, study was never initiated or activated” (63% match in meaning)

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.