CompletedPhase 4ketamine

Nebulized Sub-dissociative Dose Ketamine for Treating Pain

Sponsored by Antonios Likourezos

NCT ID
NCT03909607
Target Enrollment
120 participants
Start Date
2019-04-16
Est. Completion
2021-06-30

About This Study

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.

Conditions Studied

Pain

Interventions

  • Ketamine 0.75 mg/kg
  • Ketamine 1.0 mg/kg
  • Ketamine 1.5 mg/kg

Eligibility

Age:18 Years - 120 Years
Healthy Volunteers:No
View full eligibility 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.

Study Locations (1)

Maimonides Medical Center
Brooklyn, New York, United States

This trial is not recruiting

This study has completed enrollment. Check back for results or find similar trials.

Find recruiting trials
Data Source
ClinicalTrials.gov

Last updated from source