TRAUMA HELP: Healing and Analgesia With Propranolol

Withdrawn before enrolling · Phase 2 · Has a placebo group

Conditions studied: Trauma

In brief

The purpose of this study is to determine whether propranolol can decrease pain symptoms in a common subset of patients admitted to a trauma center after injury.

Key facts

Study ID

NCT01007084

Run by

University of North Carolina, Chapel Hill

People needed

0

Starts

2009-10-01

Expected to finish

2010-07-01

Last updated by the study team

2011-12-08

Who can join

Age: 18 and older, up to 60. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• at least one fracture
• ages 18-60 yrs
• pain score >= 4
• speak and read English

You may not qualify if…

• gunshot, stab wound, or assault
• paraplegia/quadriplegia
• pregnancy
• psychotic, suicidal, or homicidal
• hepatic, kidney failure
• clinically unstable or intubated at time of recruitment
• hyperthyroidism
• propranolol use within the last 6 months
• significant bradycardia
• cancer (except basal cell)
• peripheral vascular disease
• heart block > 1 degree
• breastfeeding
• congestive heart failure

Where it is running

• University of North Carolina Trauma Center — Chapel Hill, North Carolina, United States

Full record on ClinicalTrials.gov

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