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Aripiprazole or Ondansetron: better for Obsessive-compulsive disorder Patients

To study the efficacy and safety of aripiprazole and Ondansetron augmentation among obsessive-compulsive Disorder patients undergoing standard treatment. - NIL

Status
Active, not recruiting
Phases
Phase 3Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/11/076201
Enrollment
30
Registered
2024-11-04
Start date
Unknown
Completion date
Unknown
Last updated
2024-11-11

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

Conditions

Health Condition 1: F99- Mental disorder, not otherwise specified

Interventions

Intervention1: TAB. ONDANSETRON 4mg per oral once a day for 20 weeks Tab. ARIPIPRAZOLE 10mg per oral once a day for 20 weeks: ONDANSETRON AUGMENTATION ALONG WITH STANDARD TREATMENT IN OBSESSIVE COMPUL

Sponsors

NIL
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients of either gender Patients with age ranging between 18-60 years Patients who gave consent and were willing to participate

Exclusion criteria

Exclusion criteria: History of hypersensitivity or allergy to any of drugs we are going to use during study (Ondansetron, Aripiprazole) History of head trauma History of epilepsy History of any organic brain disease History of Schizophrenia, Bipolar Mood Disorder, Dementia, Acute Psychosis Pregnant and lactating women Liver disease Renal dysfunction Evidence of an end stage disease of a major system (hepatic, renal, respiratory, haematologic (PA), immunologic, cardiovascular, inflammatory, rheumatology, active infections, peripheral vascular disease, untreated endocrine (hypothyroid).

Design outcomes

Primary

MeasureTime frame
Aripirazole being an antipsychotic is expected to have better outcomesTimepoint: at baseline, 6 weeks, 12 weeks & 20 weeks

Secondary

MeasureTime frame
YBOCS Scale, CGI-S Scale,CGI-I Scale at 20 WeeksTimepoint: 6 weeks, 12 weeks, 20 weeeks

Countries

India

Contacts

Public ContactChandraveer Singh

UPUMS SAIFAI

cvsingh.singh@gmail.com9927791470

Outcome results

None listed

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