Reproductive Function in Women With Bipolar Disorder

NCT ID: NCT05307848

Last Updated: 2022-04-01

Basic Information

• Recruitment Status: UNKNOWN
• Total Enrollment: 200 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2021-03-01
• Study Completion Date: 2023-02-28

Brief Summary

Many studies have shown that patients with bipolar disorder are prone to reproductive dysfunction, including polycystic ovary syndrome, hyperprolactinemia, and amenorrhea. However, there is still considerable disagreement about the causes of reproductive dysfunction in patients with bipolar disorder. This study will evaluate the reproductive function of female patients with bipolar disorder without medication and those with bipolar disorder after stable medication, compared with the health control. The purpose of the study is to explore the influence, degree, and possible risk factors of bipolar disorder itself and drugs on the reproductive function of female patients.

Detailed Description

This study will comprise 60 female patients with bipolar disorder without medication, 60 female patients with bipolar disorder after stable prescription for ≥6 months, and 60 age and BMI-matched healthy controls. All of whom gave informed consent. All participants will be assessed and clinically examined at baseline, and all patients are encouraged to follow up in the sixth month. Baseline assessments will include demographics, menstrual records, comprehensive medical history, anthropometric measurements (weight and height), physical examination, pelvic ultrasound, and laboratory work (e.g., reproductive hormones). The follow-up of patients will include menstrual records, pelvic ultrasound, and reproductive hormones. Clinical symptoms will be assessed by Hamilton Depression Scale, Hamilton Anxiety Scale, and Young Mania Rating Scale at baseline and week 24. The cognitive function will be assessed at baseline and the sixth month with the Reusable Assessment of Neuropsychological Status Battery (RBANS) and the Stroop Color-Word Test. The primary outcomes will be menstruation, reproductive hormone levels, and pelvic ultrasound. Secondary outcomes will include overall psychiatric symptomatology, quality of life, cognitive function, and other biological data.

Conditions

Bipolar Disorder

Study Design

• Observational Model Type: COHORT
• Study Time Perspective: PROSPECTIVE

Study Groups

Female patients with bipolar disorder without medication

No intervention

Intervention Type: OTHER

No intervention

Female patients with bipolar disorder after stable prescription for ≥6 months

No intervention

Intervention Type: OTHER

No intervention

Age and BMI-matched healthy controls

No intervention

Intervention Type: OTHER

No intervention

Interventions

No intervention

No intervention

Intervention Type: OTHER

Eligibility Criteria

Inclusion Criteria

• Test groups：

1. Subjects voluntarily participated in the trial and signed informed consent and were able to comply with planned visits, laboratory tests, and other study procedures；

2. Meets the diagnostic criteria for bipolar disorder in the DSM-5 (Diagnostic and Statistical Manual of Mental Disorders, 5th Edition) and has no coexisting psychiatric disorders；

3. First diagnosis of bipolar disorder or stable medication for ≥6 months.

• Control group：

1. Subjects voluntarily participated in the trial and signed informed consent and were able to comply with planned visits, laboratory tests, and other study procedures；

2. No history of mental illness;

3. No history of psychotropic medication.

Exclusion Criteria

1. Presence of any other medical disorder affecting reproductive endocrine function;

2. Taking contraceptives, immunosuppressants, and other drugs that may affect reproductive function within six months;

3. Currently pregnant, breastfeeding, or planning to become pregnant in perimenopause or postmenopause;

4. Those with obvious suicidal tendencies;

5. Serious neurological disease with a clear family history or underlying risk;

6. Combining other severe acute or chronic diseases, mental diseases, or abnormal laboratory tests has clinical significance, and the subject is judged by the investigator to be unsuitable to participate in this study.

• Minimum Eligible Age: 16 Years
• Maximum Eligible Age: 40 Years
• Eligible Sex: FEMALE
• Accepts Healthy Volunteers: Yes

Sponsors

Central South University

OTHER

Sponsor Role: lead

Responsible Party

Renrong Wu

Professor

Responsibility Role: PRINCIPAL_INVESTIGATOR

Locations

Mental Health Institute of 2nd Xiangya Hospital,CSU

Changsha, , China

Site Status: RECRUITING

Countries

China

Central Contacts

Jindong Chen, M.D. Ph.D

Role: CONTACT

chenjindong@csu.edu.cn

+8613807319266

Jing Huang, M.D. Ph.D

Role: CONTACT

jinghuangserena001@csu.edu.cn

Facility Contacts

Jing Huang, PhD

Role: primary

jinghuangserena001@csu.edu.cn

15874290980

Other Identifiers

RF20220301

Identifier Type: -

Identifier Source: org_study_id