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Comparison of topiramate and placebo in controlling the OCD symptoms of bipolar patients

Comparison of treatment of bipolar disorder (lithium + olanzapine + clonazepam) and placebo with a treatment regimen containing topiramate in controlling the OCD symptoms of bipolar patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2012061310013N1
Enrollment
32
Registered
2012-10-05
Start date
2012-07-22
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Condition 1: Bipolar Mood Disorder. Condition 2: Obsessive-Compulsive disorder. Bipolar affective disorder, current episode hypomanic Predominantly obsessional thoughts or ruminations

Interventions

Intervention 1: 16 patient intervention group will recieve topiramate in addition to lithium,olanzapine and clonazepam for 16 weeks.Dose of lithium, olanzapine, and clonazepam will sufficient for pati
Treatment - Drugs
Placebo
16 patient intervention group will recieve topiramate in addition to lithium,olanzapine and clonazepam for 16 weeks.Dose of lithium, olanzapine, and clonazepam will sufficient for patients symptoms co
16 patients control group will recieve placebo in addition to lithium,olanzapine and clonazepam for 16 weeks.Dose of lithium, olanzapine, and clonazepam will sufficient for patients symptoms control.p

Sponsors

Shiraz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Inclusion criteria: Fulfilling DSM-IV-TR criteria for bipolar mood disorder; have not Major medical problem ( cardiovascular, respiratory, renal or gastrointestinal disease); not pregnant; not alcohol or other substances abuser; scores >= 18 in Yale- Brown Obsessive Compulsive Scale questionnaire. Exclusion criteria; failure to cooperate in the ongoing project for the periodical visits; non-qualification for inclusion criteria.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Obsessive-compulsive signs&symptoms in BMD patients. Timepoint: before intervention and then monthly for 4 months. Method of measurement: Yale- Brown Obsessive Compulsive Scale questionaire.

Secondary

MeasureTime frame
Drug side effects. Timepoint: monthly for 4 months. Method of measurement: checklist of drug side effects.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAli Sahraian, MD

Psychiatry department of Shiraz University of Medical Sciences

sahraian@sums.ac.ir+98 71 1627 9319

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026