Autopsy report · NCT00464386

Continuous Glucose Monitoring (POC) in the ICU

“Study device required infeasible modifications. No patients received device.”

The sponsor’s own words in the registry.

Life of this trial

• Registered 7 months after it had already started.
• Ran for about 7 years 3 months before it stopped.
• 23 participants enrolled.
• No results are posted on the registry.

Vital statistics

Status

Terminated

Phase

Na

Sponsor

United States Army Institute of Surgical Research

Sponsor type

US federal agency

Conditions

Burns; Trauma

Interventions

Continuous Glucose Monitoring

Participants

23

Sites

1

Countries

United States

Trials that died the same way

• Functional Assessment of a Vibration Feedback on the Gripping Pressure in the Territory of the Median Nerve
  “Technical problem with one of the medical device used for the study.” (66% match in meaning)
• An in Vivo Comparison of the Debridement Efficiency of Needle Irrigation Versus Ultrasonic Irrigation
  “Manufacturer changed device so no study will be done; ie it was never started” (64% match in meaning)
• Gynecare TVT Secur for the Management of Stress Urinary Incontinence (SUI)
  “Study design required a change in device” (63% match in meaning)
• Sensory Responses to Dorsal Root Stimulation
  “No participant/patient opportunities for testing. Received funding for a different study.” (62% match in meaning)
• Hepatic Artery Infusion (HAI) Program at Duke University
  “No subjects enrolled due to availability of device commercially.” (62% 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.