A Study of Olanzapine in Participants With Bipolar Disorder.
Recruiting now
Conditions studied: Bipolar Disorder
In brief
This study aimed to identify treatment patterns in patients with bipolar disorder receiving olanzapine according to demographic and clinical characteristics and to evaluate the effectiveness of education on weight gain, a side effect of olanzapine, in preventing weight gain.
Key facts
- Study ID
- NCT07263191
- Run by
- Boryung Pharmaceutical Co., Ltd
- People needed
- 3000
- Starts
- 2025-10-30
- Expected to finish
- 2027-09-01
- Last updated by the study team
- 2025-12-04
Who can join
Age: 19 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Patients who have signed the informed consent after receiving information about the purpose and method of this study.
- Patients diagnosed with bipolar disorder and scheduled to receive olanzapine.
- Patients who understand the contents of the survey and can answer the questions directly.
You may not qualify if…
- Female patients who are pregnant, have childbearing potential, or are breastfeeding.
- Has received an investigational product within 12 weeks from the study enrollment or has plans to participate in another clinical trial during the participation of this study.
- Other subjects who are considered inappropriate to participate in this study by the judgment of the investigator.
Where it is running
- CHA Bundang Medical Center — Seongnam, South Korea (enrolling)
Full record on ClinicalTrials.gov
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