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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04963257
Other study ID # 2019-234
Secondary ID
Status Recruiting
Phase Phase 4
First received
Last updated
Start date January 1, 2020
Est. completion date December 31, 2024

Study information

Verified date June 2021
Source Second Affiliated Hospital, School of Medicine, Zhejiang University
Contact Zheng Lin, Doctor
Phone 13757118261
Email linzzr@126.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

To verify that sertraline combined with fluvoxamine is superior to sertraline combined with aripiprazole


Description:

To verify that sertraline combined with fluvoxamine is superior to sertraline combined with aripiprazole, and to observe the indicators of improving patients' cognitive function and adverse drug reactions, so as to provide evidence-based evidence for supplementing the treatment guidelines for obsessive-compulsive disorder


Recruitment information / eligibility

Status Recruiting
Enrollment 400
Est. completion date December 31, 2024
Est. primary completion date December 31, 2023
Accepts healthy volunteers No
Gender All
Age group 12 Years to 45 Years
Eligibility Inclusion Criteria: - The Diagnostic criteria of OCD in the Diagnostic and Statistical Manual of Mental Disorders 5th edition (DSM-V), as well as the definition of refractory OCD, are as follows: failure to respond to oral treatment with at least two effective doses of antidepressants, including: Fluoxetine (=20mg/ d), fluvoxamine (=200mg/d), sertraline (=150mg/d), and paroxetine (= 40mg/d) were all treated for at least 12 weeks. The Yale-Brown compulsive scale (Y-BOCS) score decreased by < 35%. - The total score of Yale- Brown compulsion scale (Y-BOCS) =16 points. (3)age 12 ~ 45 years. Exclusion Criteria: - Exclusion of severe organic brain disease; - Severe physical illness; - Other mental disorders such as tics, disruptive disorders, eating disorders and autism spectrum disorders; - Pediatric streptococcal infection causedby autoimmune neuropsychiatric disease (PANDAS); - Alcohol and drug dependence; Angle-closure glaucoma; - Suicidal tendencies; - Previous history of drug allergies related to research; - Pregnant and lactating women.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
sertraline fluvoxamine
the initial dose of sertraline was given 50mg/d and the initial dose of fluvoxamine was 50mg/d, and the target dose of sertraline was gradually increased to 200mg/ d and the target dose of fluvoxamine was 200-300mg/d within 2 weeks, and the specific dose adjustment process was determined by the doctors on the basis of patients' conditions
sertraline
The initial dose of sertraline was 50mg/d and the initial dose of aripiprazole was 5mg/d. The target dose of sertraline was 200mg/ d and the target dose of aripiprazole was 5-20mg/d within 2 weeks, and the specific dose adjustment process was determined by the doctors on the basis of patients' conditions

Locations

Country Name City State
China The Fourth Affiliated Hospital of Zhejiang University Medical College Yiwu Zhejiang

Sponsors (1)

Lead Sponsor Collaborator
Second Affiliated Hospital, School of Medicine, Zhejiang University

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Y-BOCS score Treatment effectiveness was defined as a reduction of =35% in Y-BOCS score compared to baseline(12 weeks). Treatment recovery: Y-BOCS score below 8 (12 weeks) 12 weeks
Primary Ratio of Y-BOCS score reduction from baseline Treatment effectiveness was defined as a reduction of =35% in Y-BOCS score compared to baseline(12 weeks). 12 weeks
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