Autopsy report · NCT05148117

Mitochondrial Dysfunction Contributes to Sepsis Induced Cardiac Dysfunction

“Could not get through IRB submission and co-investigators with needed skillsets for study departed organization”

The sponsor’s own words in the registry.

Life of this trial

• Withdrawn before it enrolled anyone. Its dates are the sponsor's plans, not events that happened.

Vital statistics

Status

Withdrawn

Sponsor

University of Alabama at Birmingham

Sponsor type

University, hospital or other

Conditions

Sepsis

Interventions

Suspected Sepsis Group - Diagnostic Measurements; Control Group - Diagnostic Measurements

Participants

0

Sites

1

Countries

United States

Trials that died the same way

• Calm for Cancer Patients Receiving Chemotherapy
  “Study was never submitted to the IRB so never received permission to or enrolled any subjects” (69% match in meaning)
• Adherence to Otezla
  “Terminated IRB approval 6/26/2024, study was never initiated or activated” (65% match in meaning)
• Safety of Topical Tranexamic Acid in Total Joint Arthroplasty in High Risk Patients
  “Study did not receive IRB approval, so did not start” (65% match in meaning)
• Methadone as an Alternative Treatment for Children Underdoing HSCT
  “Study is closed with the IRB due to no funding. May resume once funding is obtained.” (63% match in meaning)
• Exhaled Breath Condensate pH in Patients With Cough Caused by Gastroesophageal Reflux
  “IRB approval not renewed/approval lapsed. Prior status: insufficient enrollment; study suspended pending analysis” (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.