A Case-Control Study of Gut and Vaginal Microbiota Differences Between Premature Ovarian Insufficiency Patients and Healthy Controls

Status: Recruiting
Location: See all (2) locations...
Study Type: Observational
SUMMARY

This study investigates the differences in gut and vaginal microbiota between women with premature ovarian insufficiency (POI) and healthy volunteers. POI refers to the reduction in ovarian function before the age of 40, leading to irregular or absent menstruation and decreased estrogen levels, which can significantly affect women's reproductive and overall health. Recent research has suggested that gut microorganisms may influence the balance of steroid hormones through various metabolic pathways. Additionally, certain vaginal bacteria appear enriched in patients with POI, but whether these microorganisms directly impact ovarian function, and how, remains unclear. This study also seeks to address the underexplored role of fungi within the human microbiome. To comprehensively compare differences in gut and vaginal microbiota, the study will recruit 20 women with POI and 20 healthy controls. Both demographic and clinical information will be collected, along with biological samples including blood, urine, stool, and vaginal swabs.

Eligibility
Participation Requirements
Sex: Female
Minimum Age: 20
Maximum Age: 40
Healthy Volunteers: t
View:

⁃ (For POI patients)

• Women aged 20 to 40 years at screening visit.

• Clinical diagnosis of premature ovarian insufficiency (based on diagnostic criteria: 25 \< FSH ≤ 40 IU/L, reduced follicle count and abnormal follicle development by ultrasound).

• Able to provide informed consent.

⁃ (For healthy volunteers)

• Age (±2 years) and sex-matched healthy control individuals for each POI patient.

• Able to provide informed consent.

Locations
Other Locations
China
Shanghai Changzheng Hospital
RECRUITING
Shanghai
The Ruijin Hospital Affiliated to Shanghai Jiao Tong University School of Medicine
RECRUITING
Shanghai
Contact Information
Primary
Jusheng Zheng, PhD
zhengjusheng@westlake.edu.cn
86-0571-86915303
Time Frame
Start Date: 2025-05-13
Estimated Completion Date: 2026-01-30
Participants
Target number of participants: 40
Treatments
POI
Premature ovarian insufficiency
CTL
Healthy control
Related Therapeutic Areas
Sponsors
Leads: Westlake University

This content was sourced from clinicaltrials.gov