Safety and Efficacy of Pramipexole Treatment in Resistant Obsessive-Compulsive Disorder (OCD): Pilot, Randomized and Controlled Clinical Trial

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 2
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.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 64
Healthy Volunteers: f
View:

⁃ Age between 18 and 64 years;

⁃ European Portuguese as mother tongue;

⁃ Patients diagnosed with OCD, regardless of subtype, according to DSM-5 and/or ICD-10 criteria;

⁃ Yale-Brown Obsessive Compulsive Scale (Y-BOCS) score ≥ 16;

⁃ Patients resistant to the first-line treatment for OCD:

• 1 Patients who do not respond to treatment with at least two selective serotonin reuptake inhibitor antidepressants (SSRIs) at the maximum tolerated therapeutic dose during at least 12 weeks, i.e. patients in whom there is no reduction in the Y-BOCS score by 25% relative to the score obtained before starting treatment with SSRIs.

• 2 Patients who do not respond to treatment with risperidone or aripiprazole as potentiation of the SSRIs at the maximum tolerated therapeutic dose during at least 12 weeks, i.e. patients in whom there is no reduction in the Y-BOCS score by 25% relative to the score obtained before starting treatment with the antipsychotic or patients in whom the Y-BOCS score is kept ≥ 16 after the treatment with the antipsychotic.

Locations
Other Locations
Portugal
Clinical Academic Center - Braga (2CA-Braga)
RECRUITING
Braga
Contact Information
Primary
Mónica Gonçalves
2ca@ccabraga.org
+351 253 027 249
Backup
Joana Reis
cro@ccabraga.org
+351 253 027 249
Time Frame
Start Date: 2024-08-20
Estimated Completion Date: 2028-08-20
Participants
Target number of participants: 48
Treatments
Experimental: Pramipexole at a dose of 0.088 mg/tid
Treatment with antidepressant and pramipexole at a dose of 0.088 mg/tid (0.125 mg of salt)
Experimental: Pramipexole at a dose of 0.18 mg/tid
Treatment with antidepressant and pramipexole at a dose of 0.18 mg/tid (0.25 mg of salt)
Experimental: Pramipexole at a dose of 0.35 mg/tid
Treatment with antidepressant and pramipexole at a dose of 0.35 mg/tid (0.50 mg of salt)
Related Therapeutic Areas
Sponsors
Leads: Clinical Academic Center (2CA-Braga)

This content was sourced from clinicaltrials.gov