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Pilot Study of RR-HNK in OCD

RecruitingPhase 1, Phase 2Ages 18 Years - 65 YearsAllCarolyn Rodriguez
NCT06575075 on ClinicalTrials.gov ↗
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In plain words

What the trial is, and whether it could suit you

The purpose of this study is to understand how RR-HNK works in the brain to bring about a reduction in OCD symptoms.

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📋 Eligibility rules (as published)
Inclusion Criteria: * Ages 18-65 * Meet the criteria for OCD diagnosis * Failed at least 1 prior trial of standard first-line OCD treatment (e.g. SRI/CBT) or or had refused these treatments for individual reasons * Agree to the following lifestyle modifications: comply with requirements for fasting prior to --the infusion session, not enroll in any other interventional clinical trials during the duration of the study, and commit to medication study procedures. * Able to provide informed consent Exclusion Criteria: * Allergy or hypersensitivity to ketamine * Any current or past medical/psychiatric condition that makes participation unsafe in the opinion of the investigator or study physician * Pregnant or nursing, or able to become pregnant and are not practicing an effective means of birth control * Lifetime history of deep brain stimulation
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What it tests

  • RR-HNK/Hydroxynorketamine
  • Placebo
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Where

1 site
Stanford University School of Medicine
Palo Alto, United States
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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