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

Last updated: January 3, 2025
Sponsor: Clinical Academic Center (2CA-Braga)
Overall Status: Active - Recruiting

Phase

2

Condition

Obsessive-compulsive Disorder

Anxiety Disorders

Panic Disorders

Treatment

Pramipexole 0.18 mg/tid

Pramipexole 0.088mg/tid

Pramipexole 0.35 mg/tid

Clinical Study ID

NCT06611592
OCD_rt
2024-511085-37-00
  • Ages 18-64
  • All Genders

Study 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 Criteria

Inclusion

Inclusion Criteria:

  1. Age between 18 and 64 years;

  2. European Portuguese as mother tongue;

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

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

  5. Patients resistant to the first-line treatment for OCD:

5.1 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.

5.2 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.

Exclusion

Exclusion Criteria:

  1. Patients with current or anterior history of psychotic illness (schizophrenia,delusions, among others);

  2. Patients with bipolar disorder;

  3. Patients with tick disorder;

  4. Patients with borderline personality disorder;

  5. Patients with social anxiety disorder;

  6. Patients with current or anterior history of dietary behavior disorders (at least inthe last 6 months);

  7. Patients with a history of neurological disease or traumatic brain injury;

  8. Patients with history of alcohol abuse or illicit substances (at least in the last 6months);

  9. Patients who are passing or have passed in the last 6 months by a major depressiveepisode;

  10. Patients that undergo deep brain stimulation;

  11. Presence of sensory deficits impeding participation in clinical study;

  12. Pregnant or in breastfeeding period;

  13. Patients who are doing or have done psychotherapy in the last 6 months;

  14. Patients doing medication or receiving prohibited treatments;

  15. Patients with allergy to pramipexole or any of the excipients;

  16. Patients with creatinine clearance ≤ 50 ml/min (calculated by Cockcroft-Gaultformula);

  17. Patients with NYHA III or IV heart failure or any other severe cardiovasculardisease;

  18. Hypotension (<90/60 mmHg) sitting position and hypotension orthostatic (drop insystolic AT ≥20 mmHg or diastolic AT ≥10 mmHg after 2-3 minutes of orthostatism) atthe screening;

  19. Patients with contraindication to perform MRI cannot participate in the assessmentof the exploratory endpoint (i.e., other pre-specified outcomes).

Study Design

Total Participants: 48
Treatment Group(s): 3
Primary Treatment: Pramipexole 0.18 mg/tid
Phase: 2
Study Start date:
August 20, 2024
Estimated Completion Date:
August 20, 2028

Study Description

Phase 2 clinical trial, randomized, with three-parallel-groups, lasting 26 weeks (screening phase, 4 weeks + treatment phase, 16 weeks + follow-up phase, 6 weeks), whose primary objective is to evaluate the effectiveness of using pramipexole as a strategy for boosting SSRIs, in three different doses, in treatment of resistant OCD.

The main endpoint is the measurement of the difference in the total score of the Y-BOCS scale between baseline (V1; before intervention with the investigational drug) and week 16 (V9; after intervention with the investigational drug), between the different groups treated with different doses of pramipexole.

Connect with a study center

  • Clinical Academic Center - Braga (2CA-Braga)

    Braga, 4710-243
    Portugal

    Active - Recruiting

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