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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05706922
Other study ID # NL80648.078.22
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date November 16, 2023
Est. completion date December 2024

Study information

Verified date February 2024
Source Erasmus Medical Center
Contact Xu Shan Gao, drs.
Phone +31631016348
Email x.gao@erasmusmc.nl
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Polycystic ovary syndrome (PCOS) is an endocrine disorder that affects up to 10% of the reproductive-aged women worldwide. The etiology is still unknown and treatment therefore remains symptomatic. Studies indicate a possible role of the gut microbiome in the pathology of PCOS. PCOS women have a disturbed gut microbiome, with certain species associated with the PCOS characteristics:hyperandrogenism, ovarian dysfunction, obesity, glucose intolerance and insulin resistance. Although differences have been found in gut microbiome composition between PCOS and healthy women, the literature is inconclusive regarding the difference in gut microbiome biodiversity. Studies examining the vaginal microbiome in PCOS women show consistent results with specific species in the vaginal microbiome. However, there are only few studies on the vaginal microbiome in PCOS women and no studies have yet investigated the correlation between sex-specific hormones and PCOS characteristics. More research is needed to understand the function of the microbiome in the pathophysiology of PCOS, so that this can offer perspectives in future therapies.


Recruitment information / eligibility

Status Recruiting
Enrollment 200
Est. completion date December 2024
Est. primary completion date June 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 45 Years
Eligibility Inclusion criteria - Caucasian - Willing to provide vaginal swab and stool sample - Willing to provide informed consent - Sufficient command of the Dutch language - Diagnosed with PCOS at Erasmus MC using the Rotterdam criteria by the presence of at least two of the following criteria - Clinical or biochemical hyperandrogenism (modified Ferriman-Gallway score >5; testosterone level >2nmol/L, Free Androgen Index > 2.9) - Oligomenorrorrhea or amenorrhea - Polycystic ovaries. Exclusion criteria - BMI <18 - Smoking - Diabetes Mellitus or use of insulin sensitizer - Chronic and acute infection diseases - Endometriosis (American Fertility Score (AFS) III/IV) - Elevated prolactin levels, thyroid disease, Cushing disease or gastro-intestinal disease - The use of hormonal contraceptives, and other steroid hormones in the last 3 months - Use of antibiotics, probiotics or laxatives in the last 3 months

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Venous blood sample, vaginal swab
Venous blood samples and vaginal swab will be obtained on the same day.

Locations

Country Name City State
Netherlands Erasmus University Medical Center Rotterdam South-Holland

Sponsors (1)

Lead Sponsor Collaborator
Erasmus Medical Center

Country where clinical trial is conducted

Netherlands, 

Outcome

Type Measure Description Time frame Safety issue
Primary Bacterial composition of the gut in women with PCOS and control group Bacterial composition in the gut is analysed using 16S rRNA gene sequencing 1 week
Secondary Bacterial composition of the vagina in women with PCOS and control group Bacterial composition in the vagina is analysed using 16S rRNA gene sequencing 1 week
Secondary Difference in bacterial composition of the vagina and gut in women with PCOS Relative abundance of bacterial communities 1 week
Secondary Difference in bacterial composition of the vagina and gut between overweight/obese and lean patients (with/without PCOS) Relative abundance of bacterial communities 1 week
Secondary To analyse potential metabolic profiles characterizing different phenotypes of PCOS Expression of metabolic indicators (metabolomics) 1 week
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