Study on how genetics and microbiome affect OCD treatment with SSRIs
Official title: Pharmaco(Epi)Genetic, Proteomic, and Microbiomic Study of Obsessive-Compulsive
Run by Severance Hospital · NCT02431845 · Data updated 2026-11-12
This study is testing how genetics and gut bacteria might influence how well people with obsessive-compulsive disorder respond to a common medication called SSRIs.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 19 Years to 70 Years |
| Sex | All |
| Enrollment | 200 (estimated) |
| Sponsor | Severance Hospital Academic / other |
| Locations | 1 site (Seoul) |
| Status | Recruiting |
| Started | January 1, 2013 |
| Main results expected | December 31, 2030 |
| Study ends | December 31, 2030 |
| Registry record updated | December 27, 2024 |
| Trial ID | NCT02431845 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are adults aged 19 to 70 with a diagnosis of OCD who are drug-naive or have been drug-free for more than three months.
✕Probably not a fit
Patients with neurological disorders, comorbid psychotic disorders, or substance dependence within the past six months 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 study aims to investigate the relationship between genetic variants, microbiome, and the response to selective serotonin reuptake inhibitors (SSRIs) in patients with obsessive-compulsive disorder (OCD). It will recruit 200 drug-naive or drug-free participants aged 19 to 70, who will receive SSRIs tailored to their individual needs. Evaluations will be conducted at baseline, 4 months, 6 months, and 1 year after treatment using various psychological scales and functional MRI for some participants. Blood samples will be collected for genetic, proteomic, and microbiomic analyses to explore predictors of treatment response.
Why it matters
Potential benefit: If successful, this study could lead to personalized treatment strategies for OCD, improving patient outcomes.
How similar studies have gone: While there have been studies on SSRIs and OCD, the specific integration of (epi)genetics and microbiome analysis in this context is relatively novel.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: 1. age 19\~ 70 2. OCD by Diagnostic and Statistical Manual for Mental disorders, 4th edition (DSM-IV) 3. drug naive or drug free for more than 3 months Exclusion Criteria: 1. any neurological disorder 2. comorbid psychotic disorders 3. alcohol or other substance dependence within past 6 months 4. any evidences for brain diseases
Where it's running
-
Yonsei Univ. Health System Severance Hospital
Seoul, South Korea Recruiting
Study contacts
- Principal investigator: Se Joo Kim, M.D. — Professor, Department of Psychiactry, Yonsei Univ. College of Medicine
- Study coordinator: Se Joo Kim, M.D.
- Email: kimsejoo@yuhs.ac
- Phone: +82-2-2228-1627
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
-
Low-intensity focused ultrasound targeting the subthalamic nucleus for OCD
A short test is being done to see if a wearable, non-invasive ultrasound device can safely and tolerably help adults with OCD by targeting a brain region called the subthalamic nucleus.
-
Mindfulness-Based Cognitive Therapy for OCD Delivered Online
This study tests a synchronous online MBCT program for adults with OCD to see if it is acceptable and feasible and to explore links between biological markers, OCD severity, and treatment response.
-
Targeted brain stimulation for OCD: test of tTIS on nucleus accumbens
This study tests whether targeted temporal interference stimulation of the nucleus accumbens can help reduce obsessive-compulsive symptoms in adults with OCD, compared with sham stimulation.
-
Anxiety Skills Study: See if video skill training plus therapy helps people with anxiety
This study tests whether a brief video-based skill training can help people with anxiety as well as four therapy sessions, and how durable the effects are over a year.
-
AttunE LIFU for OCD: a non-invasive brain stimulation study
This trial tests ATTN201, a wearable ultrasound headband, to see if it helps adults with OCD compared to a sham treatment.
-
Combined ERP and Habit Reversal Therapy for Tourettic OCD
This study tests whether a merged Exposure and Response Prevention and Habit Reversal Therapy helps adults with Tourettic OCD more than either therapy alone or basic psychoeducation.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.