Investigating (2R,6R)-HNK for Acute Pain
This study is looking into a new experimental drug called (2R,6R)-hydroxynorketamine (HNK) to see if it can help reduce short-term pain in healthy adults. Opioid pain medications can be addictive, and researchers are searching for new options. HNK is related to ketamine and may offer pain relief with fewer side effects. You might be able to join if you are a healthy adult between 18 and 60 years old. The main goal is to see if a single dose of HNK can reduce pain during special tests. This study aims to understand if HNK has pain-relieving effects and how it works in the brain, which could lead to new pain treatments.
- Study design
- This is a randomized, double-blind (you and your doctor won't know if you're getting the drug or placebo), placebo-controlled study involving 92 healthy volunteers.
- What's involved
- You will receive a single intravenous (IV) infusion of either HNK or a placebo over about 40 minutes. You will have inpatient and outpatient visits.
- Compensation
- Not stated in the trial record.
- Follow-up
- Pain ratings will be measured at 3-5 hours after the infusion, and secondary outcomes will be assessed immediately after infusion, after 4-5 hours, and one day later.
AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.
Investigating the Analgesic Potential of (2R,6R)-HNK in Acute Pain in Healthy Volunteers
At a glance
Conditions
NCT07504601
Where you'd take part
This study runs at 1 site. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.
National Institutes of Health Clinical Center
Bethesda, Marylandstudy coordinator listed
Sites open and close at different times, so the status above is per site — it can differ from the study's overall status.
Study leadership
- Lauren Y Atlas, Ph.D. · PRINCIPAL_INVESTIGATOR · National Center for Complementary and Integrative Health (NCCIH)
Who to contact
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What this trial measures
- Pain ratings during quantitative sensory testing (QST)3-5 hours after infusion
Change in pain intensity ratings in response to experimentally induced nociceptive stimuli during quantitative sensory testing (QST), comparing (2R,6R)-hydroxynorketamine (HNK) with placebo in a randomized, double blind crossover design, controlling for baseline pain sensitivity.