Oxytocin and Oxycodone for Pain and Abuse Liability

This study is exploring if oxytocin nasal spray, when given with oxycodone (an opioid pain medication), can reduce oxycodone's potential for abuse and improve its pain-relieving effects. Researchers will give participants different combinations of oxycodone (5 mg or 2.5 mg oral tablets) and oxytocin nasal spray (48 IU), or placebos (inactive substances), to see how they affect pain and other responses. You might be eligible if you are between 21 and 45 years old, use opioids recreationally, are in good general health, and do not have chronic pain. The main goal is to understand how oxytocin affects the likelihood of oxycodone abuse. The study plans to enroll 45 participants, but its current status is unclear.

Study design
This is a double-blind, randomized, placebo-controlled study where participants will receive different treatments across multiple sessions. It involves 45 participants and is designed to compare the effects of oxytocin and oxycodone, both alone and in combination.
What's involved
You would participate in a 6-session laboratory study. This includes a medical history review, a screening session, and self-administering intranasal oxytocin or placebo shortly after oral oxycodone or placebo.
Compensation
Not stated in the trial record.
Follow-up
The primary endpoint, subject-rated abuse liability, will be measured at up to 6 weeks.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT04218409

Opioid-Sparing and Pain-Reducing Properties of Syntocinon: A Dose-Effect Determination

Recruiting
EARLY_PHASE1Ages 21–45InterventionalBasic science
University of Florida
~45 participants
Updated 2026-01-14 on ClinicalTrials.gov
What's tested:OxyCODONE 5 mg Oral TabletOxytocin nasal sprayPlacebo OxycodonePlacebo oxytocinOxyCODONE 2.5 mg Oral Tablet

At a glance

Recruiting sites
1 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Subject-rated abuse liability
Measured over up to 6 weeks.
Pain
1 sites across 1 states
Florida1
  • Meredith Berry, PhD · PRINCIPAL_INVESTIGATOR · University of Florida

Opens a ready-to-send draft in your own email app — review before sending.

Do you actually qualify for this trial?

Add a private profile and we'll compare every criterion below against your situation — and tell you which ones are met, uncertain, or excluding.

Check eligibility for this trial ~2 min · HIPAA-protected · delete anytime
Eligibility criteria

Inclusion

Individuals fluent in English will participate.
Must report recreational use of opioids.
Be within 20% of their ideal body weight.
Are not currently experiencing chronic pain (pain on most days during the past 3 months)
Have a systolic blood pressure of \<=140 and diastolic blood pressure of \<= 90, and a heart rate \<= 90 beats per minute.
Participants must also have a normal electrocardiogram (EKG) reading and bloodwork indicating no major health contraindications.

Exclusion

Significant current physical disease or major psychiatric disorder.
No self-reported current interest in drug abuse treatment.
Women who are pregnant or nursing.
Any comorbid illicit substance use disorders or current clinically significant withdrawal for any abused drug excluding nicotine and caffeine.
Any conditions that preclude safety in the MRI scanner, such as: implanted electrical devices (e.g., cardiac pacemaker, neurostimulator); implanted metallic clips or pins (e.g., aneurysm clip); a history of working with metal (unless able to demonstrate participant is MRI safe), and claustrophobia.
  • Subject-rated abuse liabilityup to 6 weeks.

    Using a Visual Analog Scale with scoring as 0=not at all, 20=possibly mild, 40=definitely mild, 60=moderately, 80=strongly, and 100=extremely, or any number in between. Testing occurs only in the context of 4 sessions due to a minimum of a one week washout period in between each session.