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The effect of Ondansetron to tretment obsessive -copmpulsive disorder

The effect of Ondansetron augmentation in tretment resistant obsessive-copulsive disorder

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20170723035247N1
Enrollment
40
Registered
2018-01-03
Start date
2017-06-22
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

Obsessive -compulsive disorder. F42-The essential feature is recurrent obsessional thoughts or compulsive acts.obsessional thoughts are ideas,images,or impuses that enter the patients mind again and again in stereotyped form.They are , almost invariably distressing and the patient ofte

Interventions

Intervention 1: In the first intervention group: In addition to SSRIs, it is given ondansetron at an average dose of 8 mg per day for 2 weeks. Intervention 2: In the control group, with SSRIs, the pa
Treatment - Drugs
In the first intervention group: In addition to SSRIs, it is given ondansetron at an average dose of 8 mg per day for 2 weeks.
In the control group, with SSRIs, the patient will receive the same dose of placebo for 12 weeks as the original drug.

Sponsors

Vice chancellor for resaerch Kashan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Aged 18 years and over. Despite received at least three months of adequate and tolerable SSRI drugs, the scores of obsessive-compulsive scores 16 and up. No pregnancy or breastfeeding in women. No psychiatric disorder such as Bipolar in the axis 1 of psychiatry. Lack of mental retardation in the axis 2 of psychiatry. Lack of alcohol intake 6 months before the study. Lack of psychotherapy during the study.

Exclusion criteria

Exclusion criteria: Acute and severe physical illness during the study. Non-follow-up for 4 weeks. Severe complications during treatment. Not using contraceptive methods in females

Design outcomes

Primary

MeasureTime frame
Severity obsessive compulsion. Timepoint: Before the start of trial and every four weeks. Method of measurement: Yale Brown Obsessive -Compulsion Scala.

Secondary

MeasureTime frame
Sudden drug effect. Timepoint: Before the start of the trial ,the end of the first-two-fourth-sixth-eighth-twelfth weeks. Method of measurement: Interviwe and examination.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactZahra sepehrmanesh MD

Kashan University of Medical Sciences

Z.sepehrmanesh@yahoo.com+98 31 5554 9111

Outcome results

None listed

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