CompletedPhase 4ketamine

A Comparison of Proprietary Formulations of Oral Ketamine + Aspirin and Oral Ketamine Alone for Musculoskeletal Pain

NCT ID

NCT04860804

Target Enrollment

60 participants

Start Date

2021-04-22

Est. Completion

2021-12-31

About This Study

Acute Pain is one of the most frequent chief complaints and the main reason for visiting the Emergency Department (ED). The acute pain in the ED is largely prevalent across the country with recent literature demonstrating that 61-91% of patients are admitted to the ED due to a variety of acute painful syndromes. There is a lack of good options for pain control in such settings.

Conditions Studied

Pain

Interventions

•Aspirin and Ketamine
•Oral Ketamine

Eligibility

Age:18 Years - 120 Years

Healthy Volunteers:No

View full eligibility criteria

Inclusion Criteria:

* Patients age 18 and older
* acute musculoskeletal pain
* initial pain score of 5 or more on a standard 11- point (0 to 10) numeric rating scale.
* awake, alert, and oriented to person, place, and time

Exclusion Criteria:

* altered mental status,
* allergy to aspirin and ketamine,
* pregnant
* unstable vital signs (systolic blood pressure \<90 or\>180 mm Hg, pulse rate \<50 or \>150 beats/ min, and respiration rate \<10 or \>30 breaths/min)
* inability to provide consent
* consumption of Aspirin or NSAID's within 6 hours of arrival to the ED
* active PUD
* history of GI Hemorrhage
* history of renal and hepatic insufficiency
* past medical history of alcohol or drug abuse
* schizophrenia

Study Locations (1)

Maimonides Medical Center

Brooklyn, New York, United States