Clinical trial Recruiting at 1 site Phase 4 Interventional Ages 7 to 70

Using ketamine to reduce pain during minor procedures

Official title: Intranasal Ketamine as a Supplement to Local Anesthesia to Reduce Pain Associated With Minor Procedures in the Emergency Department

Run by Loyola University · NCT06284473 · Data updated 2026-11-12

This study is testing if using a nasal spray of ketamine can help reduce pain during minor procedures in the emergency department for people aged 7 to under 70.

Quick facts

PhasePhase 4
Study typeInterventional
Ages7 Years to 70 Years
SexAll
Enrollment108 (estimated)
SponsorLoyola University
Academic / other
Locations1 site (Maywood, Illinois)
StatusRecruiting
StartedMay 25, 2022
Main results expectedMay 31, 2028
Study endsMay 31, 2028
Registry record updatedOctober 3, 2025
Trial IDNCT06284473 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates include adults and children aged 7 to less than 70 who are undergoing minor procedures in the emergency department.

Probably not a fit

Patients with altered mental status, pregnancy, or a history of psychiatric illness may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This clinical trial evaluates the effectiveness of intranasal ketamine as a supplement to local anesthesia for pain management during minor procedures in the emergency department. Participants, aged 7 to under 70, will be randomly assigned to receive either ketamine or a saline placebo alongside standard local anesthesia. The primary goal is to compare pain scores between the two groups using a numerical rating scale, while secondary outcomes will assess agitation in adults and alertness in children. This approach aims to improve patient comfort and procedural experiences in the ED.

Why it matters

Potential benefit: If successful, this study could provide a more effective pain management option for patients undergoing minor procedures.

How similar studies have gone: Previous studies have shown that sub-dissociative doses of ketamine can effectively manage pain, indicating potential success for this approach.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Undergoing Minor Procedure in the ED
* Weight not to exceed 115kg

Exclusion Criteria:

* Altered Mental Status
* Pregnancy
* Breastfeeding
* Acute head or eye injury
* Intercranial Hypertension
* Hx of seizures
* Hx of chronic pain
* Unstable vital signs
* Allergy to Ketamine
* Hepatic or Renal Insufficiency
* Hx of Psychiatric Illness
* Hx of alcohol/drug abuse

Where it's running

  • Loyola University Medical Center
    Maywood, Illinois, United States
    Recruiting

Study contacts

  • Principal investigator: Trent Reed, DO — Loyola University
  • Study coordinator: Shannon Lovett, MD
  • Email: slovett@lumc.edu
  • Phone: 708-327-2549

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.