Benzodiazepines for the Reduction of Distress and Pain During and After Emergency Department Care

Stopped early · Phase 2 · Has a placebo group

Conditions studied: Acute Pain

In brief

In this proposal, the investigators will determine if a single dose of oral lorazepam reduces distress, pain severity, and need for opiate analgesics both in the ED and in the acute recovery period after discharge. The investigators will compare the lorazepam arm to a placebo arm.

Key facts

Study ID
NCT03756038
Run by
Maria Pacella
People needed
1
Starts
2019-01-25
Expected to finish
2019-03-27
Last updated by the study team
2020-03-09

Who can join

Age: 18 and older, up to 65. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

You may not qualify if…

Where it is running

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.