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To study therapeutic efficacy of aripiprazole augmentation in treatment resistant obsessive compulsive disorder

To study therapeutic efficacy of aripiprazole augmentation in treatment resistant obsessive compulsive disorder

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/04/032524
Enrollment
60
Registered
2021-04-05
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: F01-F99- Mental, Behavioral and Neurodevelopmental disorders

Interventions

Intervention1: Aripiprazole augmentation: Aripiprazole augmentation of ongoing anti -obsessive agents depending on dose. Group 1 with dose aripiprazole less than and equal to 5mg/day and in Group 2 do

Sponsors

GMC medical college
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients of ocd diagnosed as per DSM 5, further treatment resistant OCD defined as patients who have undergone trial of first line therapies that is two different SSRI in adeqaute dose for adequate duration that is 10-12 weeks. patients who did not show adequate response on Ybocs score that is more than 35 % reduction on YBOCS score for full response and more than 25% to 35% reduction for partial response were enrolled ..Aripiprazole was added to ongoing treatment. Group 1 consisted to patients with ongoing treatment plus dose of aripiprazole less than equal to 5mg/day and group 2 consisted dose or aripiprazole more than 5mg to 10mg/day along with ongoing treatment. Response was noted at 2,4,8,12 weeks using YBOCS , CGI. BABS scale was used for assessment of insight and beliefs. GAF and WHOQOL-BREF was used for assessment of quality of life and wellbeing.

Exclusion criteria

Exclusion criteria: other psychiatric disorder, pregnant females, substance abuse,any other medical illness, other OCRD such as BDD,TTM,Hoarding disorder, and those who refused to give consent.

Design outcomes

Primary

MeasureTime frame
Severity and treatment response on YBOCS,CGI scaleTimepoint: Baseline,2,4,8,12 weeks

Secondary

MeasureTime frame
Assessment of insight on BABS scaleTimepoint: At baseline and 12 weeks;quality of lifeTimepoint: quality of life at baseline and 12 weeks on WHOQOL-BREF

Countries

India

Contacts

Public ContactDr Ramandeep Kaur

Rajindra hospital

profheadpsy@yahoo.com9814913599

Outcome results

None listed

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