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Guidance Model of Standardized Treatment of Antidepressants in Bipolar Disorder

Clinical Psychopharmacology Division Institute of Mental Health, Peking University

Status
UNKNOWN
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03148535
Enrollment
100
Registered
2017-05-11
Start date
2017-06-01
Completion date
2018-12-01
Last updated
2017-05-11

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

Conditions

the Use of Antidepressants in Patients With Bipolar Depression

Brief summary

The bipolar depression patients of 18-55 years old were recruited. At the time of enrollment, the demographic, symptomatic, neuropsychological, neurobiological and genetic data was collected. After the completion of the baseline assessment and examination, the patients were given lithium carbonate or lithium carbonate combined with SSRI antidepressant treatment. Clinical evaluation was performed at 2 and 8 weeks after treatment, including the therapeutic efficacy and adverse drug reactions, and monitoring of serum lithium concentration. The patients further receive the fMRI scans after treatment for 8 weeks. Through above work, this study aimed to provide some guidance for the use of antidepressants in patients with bipolar depression.

Interventions

DRUGLithium Carbonate

bipolar depression recieve lithium Carbonate treatment

DRUGlithium carbonate combined with SSRI antidepressant treatment

lithium carbonate combined with SSRI antidepressant treatment

Sponsors

Peking University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 55 Years
Healthy volunteers
Yes

Inclusion criteria

* age 18-55 years old, bipolar depression

Exclusion criteria

* other mental illness, serious somatic illnesses, MRI contradictions.

Design outcomes

Primary

MeasureTime frameDescription
HRSD reduction ratio8 weeksHRSD reduction ratio

Countries

China

Contacts

Primary ContactJi-Tao Li, MD
ljt_102124@163.com010-62723742

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026