Overview

Nebulized Sub-dissociative Dose Ketamine for Treating Pain

Status:
Active, not recruiting
Trial end date:
2021-12-31
Target enrollment:
0
Participant gender:
All
Summary
The investigators previous research study comparing the efficacy of intravenous ketamine to morphine showed ketamine to provide equivalent relief of moderate to severe acute pain in emergency department patients. A second study by the investigators showed that increasing the time of administration of the ketamine, from a push injection to a drip infusion, will minimize the adverse effects experienced by recipients of ketamine. The investigators now aim to see if nebulized subdissociative-dose ketamine administered as a single agent in a dose of 1.5 mg/kg via Breath-Actuated Nebulizers (BAN) over 5-15 minutes will provide a better pain relief in comparison to 1 mg/kg and 0.75 mg/kg doses or if the lower doses are equally as effective.
Phase:
Phase 4
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Antonios Likourezos
Treatments:
Ketamine
Criteria
Inclusion Criteria:

- Patients age 18 and older

- acute and chronic abdominal, flank, back, musculoskeletal pain, and traumatic pain as
well as cancer pain

- initial pain score of 5 or more on a standard 11- point (0 to 10) numeric rating
scale.

Exclusion Criteria:

- altered mental status,

- allergy to ketamine,

- weight greater than 150 kg,

- unstable vital signs (systolic blood pressure <90 or>180 mm Hg,

- pulse rate <50 or >150 beats/min,

- respiration rate <10 or >30 breaths/min)

- alcohol or drug abuse

- inability to provide consent

- psychiatric illness (schizophrenia),

- recent (4 hours before) opioid use.