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Quetiapine Augmentation in Severe Obsessive Compulsive Disorder

AstraZeneca logo

AstraZeneca

Status and phase

Completed
Phase 3

Conditions

Obsessive Compulsive Disorder

Treatments

Drug: SSRI/Clomipramine
Drug: quetiapine fumarate

Study type

Interventional

Funder types

Industry

Identifiers

NCT00254735
5077/9059
D1441C09059

Details and patient eligibility

About

The purpose of the study is to evaluate the efficacy of quetiapine or placebo added to baseline treatment of SSRI/clomipramine for the treatment of OCD in adult subjects.

Enrollment

44 patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Signed informed consent, men and women aged ³18 to £65 years with diagnosis of OCD, at least 12 weeks of treatment with SSRI or clomipramine

Exclusion criteria

  • Substance abuse or dependence, female patients who are pregnant, lactating or at risk of pregnancy, known intolerance or lack of response to quetiapine, use of antihypertensive medication with changing doses

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

Trial contacts and locations

2

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Data sourced from clinicaltrials.gov

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