Autopsy report · NCT01007084

TRAUMA HELP: Healing and Analgesia With Propranolol

“Lack of eligible patient recruits/feasibility considerations.”

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• Withdrawn before it enrolled anyone.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Withdrawn

Phase

Phase 2

Sponsor

University of North Carolina, Chapel Hill

Sponsor type

University, hospital or other

Conditions

Trauma

Interventions

Propranolol; Propranolol ER; Sugar pills

Participants

0

Sites

1

Countries

United States

Trials that died the same way

• Endothelial Protection in Convalescent COVID-19 Patients
  “Lack of the eligible patients” (86% match in meaning)
• Fesoterodine on Urgency Episodes in Parkinson's Disease Population
  “Insufficient or untimely patient recruitment” (85% match in meaning)
• Efficacy of Botulinum Toxin Versus Lidocaine in Treating Masticatory Myofascial Face Pain Using Ultrasound and EMG Guided Techniques
  “Lack of eligible patients willing and able to participate” (85% match in meaning)
• Serial Evaluation of Drug-Eluting Stents Using OCT (STRUT-OCT)
  “Lack of eligible patients” (85% match in meaning)
• Neuropsychological Effects of Hydrocortisone in Patients With Partial Adrenal Insufficiency
  “Insufficient recruitment of suitable patients.” (83% 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.