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NCT07670507 · ClinicalTrials.gov registry record · Phase 2

Pilot Randomized Control Trial Comparing Oral Ketamine and Oral Oxycodone for Pain Control in Emergency Department Patients

A Phase 2 study, sponsored by Albany Medical College.

Not yet
Registry status
Phase 2
Development phase
60
Enrollment target

NCT07670507 is a Phase 2 study that has not yet begun recruiting, run by Albany Medical College. The registered enrollment target is 60 participants.

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The verdict

NCT07670507, a Phase 2 study, has not yet begun recruiting, sponsored by Albany Medical College.

NOT YET RECRUITING
Registry status
Phase 2
Development phase
60 participants
Enrollment target

Study Summary

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

Interventions

  • DRUG oxycodone
  • DRUG oral ketamine

Trial Details

FieldValue
Enrollment Target 60 participants
Start Date 2026-06-24
Est. Completion 2027-04-30
Phase Phase 2

Sponsor

Albany Medical College

52 total trials

What the Registry Record Tells You About NCT07670507

The ClinicalTrials.gov registry entry for NCT07670507 describes a study currently listed as not yet recruiting, categorized as Phase 2. The registered enrollment target is 60 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Albany Medical College, which has 52 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 2 interventions - of which oxycodone is the first listed.

NCT07670507 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT07670507 about?

NCT07670507 is a clinical study titled "Pilot Randomized Control Trial Comparing Oral Ketamine and Oral Oxycodone for Pain Control in Emergency Department Patients". 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...

What is the current status of trial NCT07670507?

This trial is currently not yet recruiting. It is a Phase 2 study. The enrollment target is 60 participants. The study started on 2026-06-24. Estimated completion is 2027-04-30.

What interventions are being tested in trial NCT07670507?

The interventions under investigation include: oxycodone (DRUG), oral ketamine (DRUG).

Who is sponsoring clinical trial NCT07670507?

This trial is sponsored by Albany Medical College, which has 52 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.