Pilot Randomized Control Trial Comparing Oral Ketamine and Oral Oxycodone for Pain Control in Emergency Department Patients
Part of paid clinical trials in Albany, New York.
- Sponsor
- Albany Medical College
- Study ID
- NCT07670507
- Phase
- PHASE2/PHASE3
- Status
- Not Yet Recruiting
Notify me when recruiting opens
Save your spot on the interest list for this study. We'll keep your details with this study so our team can follow up when recruiting opens.
Add your contact details and location so we can keep your interest tied to this study.
Conditions
- Pain Management
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 75 Years
- Healthy Volunteers
- Not accepted
Interventions
- oral ketamine — DRUGA dose of oral ketamine administered as a second line pain management medicine in the emergency department.
- oxycodone — DRUGA dose of oxycodone administered as a second line pain management medicine in the emergency department.
Study Details
The goal of this pilot randomized clinical trial is to learn if oral ketamine intervention can control pain in emergency department patients whose providers feel the need for additional pain medication. The main questions it aims to answer are: * Does oral ketamine result in a different mean change in pain scores compared with oral oxycodone? * Is there a difference in the need for additional opioid administration within 24 hours after the initial dose of study medication (oral ketamine vs oral oxycodone)? Researchers will compare oral ketamine to oral oxycodone to see if there is a difference in pain control or the need for additional opioid administration. Participants will: * Fill out a survey prior to study medication administration assessing pain scores, pain presentation, and medication history * Be randomized to and receive a dose of oral ketamine or oral oxycodone as the study medication for pain control * Fill out a survey assessing pain control, side effects, and safety outcomes * Receive follow-up phone calls at 1 and 3 months after enrollment to assess pain and opioid use
Key Dates
- Start date
- Jun 24, 2026
- Status verified
- Jun 2026
- Primary completion
- Dec 31, 2026
- Completion
- Apr 30, 2027
Study Design
- Enrollment
- 60 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: oral ketamineThe oral ketamine arm will receive a dose of oral ketamine as a second line pain medication.
- Active Comparator: oxycodoneThe oxycodone arm will receive a dose of oxycodone as a second line pain medication.
Primary Outcome Measure
Change in mean pain score [ Time Frame: This will be assessed at 30 minutes and 60 minutes after receiving the study drugs. ]
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Albany Medical Center Emergency Department | Albany | New York | 12208 | Michael Waxman, MD (PRINCIPAL_INVESTIGATOR) |
Find similar trials in Albany, NY
Related Studies
- Assessment of Morbidity and Mortality Following Serratus Anterior Plane Block (SAPB) for Unilateral Rib FracturesRecruiting · Albert Einstein College of Medicine · The Bronx, New York
- The Effect of Multimodal Pain Regimen on Use of Narcotics After Rotator Cuff Tear RepairPHASE4 · Recruiting · Montefiore Medical Center · The Bronx, New York
- Suzetrigine in Total Hip ArthroplastyPHASE3 · Recruiting · Hospital for Special Surgery, New York · New York, New York
- Transmucosal Uterosacral Electrical Stimulation for Pelvic Pain ReliefNot Yet Recruiting · Weill Medical College of Cornell University · New York, New York