drugset / Trial / NCT06611592

Safety and Efficacy of Pramipexole Treatment in Resistant Obsessive-Compulsive Disorder (OCD)

NCT06611592

Phase 2 Recruiting 48 enrolled Clinical Academic Center (2CA-Braga)
RandomizedParallel-groupTriple-blindTreatment

Summary

The most common and effective treatment for OCD is pharmacological therapy that includes selective serotonin reuptake inhibitors (SSRIs) antidepressants and, in the case of patients resistant to this approach, a combination with antipsychotics. Risperidone and aripiprazole are atypical antipsychotics that act on dopamine (D2) and serotonin receptors. Studies have shown that these drugs are effective in boosting SSRIs for the treatment of OCD in resistant patients. Currently a high percentage of people diagnosed with OCD do not respond to the existing treatments. Pramipexole is a dopaminergic receptor agonist that specifically binds to dopamine D2 and D3 receptors, having demonstrated benefit in resistant depression. The aim of this clinical trial is to explore how pramipexole can act in the treatment of OCD in resistant patients, evaluating its safety and efficacy.

Timeline

Start
2024-08-20
Primary completion
2028-08-20
Completion
2028-08-20

Drugs

EvaluationDrugModalityDoseRoute
Subject Pramipexole Unknown 0.088 mg Oral
Subject Pramipexole Unknown 0.18 mg Oral
Subject Pramipexole Unknown 0.35 mg Oral