Autopsy report · NCT07770581

Determining if the Buzzy® Personal Pain Relief Device Reduces Injection Pain of Propofol as Much as Intravenous Lidocaine in Children

“PI left institution and study activity was not continued (enrollment not complete)”

The sponsor’s own words in the registry.

Life of this trial

• Registered 2 months before it started.
• Ran for about 3 years before it stopped.
• 49 participants enrolled.
• No results are posted on the registry.

Vital statistics

Status

Terminated

Phase

Na

Sponsor

Ann & Robert H Lurie Children's Hospital of Chicago

Sponsor type

University, hospital or other

Conditions

Propofol Injection Pain in Children

Interventions

Buzzy device; Intravenous lidocaine

Participants

49

Sites

1

Countries

United States

Trials that died the same way

• UV and Bluelight Dosimetry
  “PI left institution and study has not begun enrollment.” (84% match in meaning)
• Randomized Controlled Trial (RCT) Umbilical Hernia Repair (UHR) Absorbable vs Non-absorbable Synthetic Mesh
  “study was never opened and PI now leaving institution” (82% match in meaning)
• Quality Control: A Prospective Analysis of EVD Effectiveness
  “PI left institution prior to study completion” (81% match in meaning)
• Use of Simvastatin for the Prevention of Vasospasm in Aneurysmal Subarachnoid Hemorrhage
  “Study PI left the institution and study was stopped at that time.” (81% match in meaning)
• Ultrasound for Diagnosis of Biliary Dyskinesia
  “PI left institution, study interest wained-so stopped.” (80% 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.