Ketamine Patient-Controlled Analgesia for Acute Pain

Stopped early · Phase 3

Conditions studied: Acute Pain, Multiple Trauma, Fractures

In brief

This study will compare ketamine and hydromorphone as alternative patient-controlled interventions for trauma-related pain. Patients receiving ketamine PCA are expected to require less total and breakthrough opioid and to have similar or improved objective pain scores. Patients receiving ketamine are also expected to have shorter duration of supplemental oxygen requirement, fewer episodes of oxygen desaturation, improved pulmonary toilet, lower use of antiemetics, and shorter times to first bowel movement. Ketamine is further expected to be associated with decreased intensive care unit and hospital lengths of stay, faster time to maximum allowable ambulation, decreased opioid dosage at discharge, and lower report of chronic pain syndromes.

Key facts

Study ID
NCT02062879
Run by
University of Cincinnati
People needed
20
Starts
2014-04-01
Expected to finish
2016-06-01
Last updated by the study team
2017-09-21

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

You may not qualify if…

Where it is running

Full record on ClinicalTrials.gov

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