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CompletedNCT07849166Updated Sep 30, 2026

BRCC36 and Telomerase Levels in Women With Polycystic Ovary Syndrome

An observational study in Polycystic Ovarian Syndrome (PCOS), sponsored by Cumhuriyet University. Completed at 1 site in Turkey (Türkiye). Open to female participants aged 18 Years to 43 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-09-30.

Sponsored by Cumhuriyet University · Observational

Updated Sep 30, 2026Newly registeredGo to Updates ↓
Study type
Observational
Model
Case-control
Time perspective
Cross-sectional
Enrollment
60
Ages
18 Years to 43 Years
Sex
Female
01

Study summary

This prospective observational case-control study evaluated serum BRCC36 and telomerase (TE) levels in women with polycystic ovary syndrome (PCOS) and healthy controls. Women aged 18-43 years were included. The study comprised 30 women diagnosed with PCOS according to ESHRE/ASRM criteria and 30 healthy women with regular menstrual cycles. A single 5-mL venous blood sample was collected from each participant. Serum was separated by centrifugation and stored at -80°C until analysis. Serum BRCC36 and telomerase levels were measured using commercially available enzyme-linked immunosorbent assay (ELISA) kits. The study evaluated differences in these biomarkers between women with PCOS and healthy controls and their relationships with clinical and biochemical characteristics.

Read the detailed description

This prospective observational case-control study included women aged 18-43 years with polycystic ovary syndrome (PCOS) and healthy controls. PCOS was diagnosed according to ESHRE/ASRM criteria based on the presence of at least two of the following features: oligo- and/or anovulation, clinical and/or biochemical hyperandrogenism, and polycystic ovarian morphology on ultrasonography.

Participants underwent clinical and anthropometric evaluation, including body mass index and modified Ferriman-Gallwey scoring. Available biochemical and hormonal parameters obtained during routine clinical evaluation were also recorded.

For the study-specific biomarker analyses, a single 5-mL venous blood sample was collected from each participant into a serum separator tube. Samples were centrifuged at 3000 rpm for 10 minutes, and the separated sera were stored at -80°C until analysis. Serum BRCC36, a deubiquitinating enzyme-related biomarker, and telomerase (TE) levels were measured using commercially available human ELISA kits.

The primary objective was to compare serum BRCC36 and telomerase levels between women with PCOS and healthy controls. Associations between these biomarkers and clinical and biochemical characteristics were also evaluated.

02

Conditions studied

  • Polycystic Ovarian Syndrome (PCOS)

Keywords

  • BRCC36
  • Telomerase
  • Deubiquitinating Enzymes
  • Polycystic Ovary Syndrome
  • Biomarkers
03

In context

Polycystic Ovary Syndrome

944 studies on the registry are indexed under Polycystic Ovary Syndrome; 175 are open to participants now.

This study's enrollment of 60 is below the median of 118 across 223 observational studies indexed under Polycystic Ovary Syndrome.

Browse Polycystic Ovary Syndrome studies →

Lead sponsor

Cumhuriyet University is the lead sponsor of 128 studies on the registry; 25 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 43 Years
Sexes eligible
Female
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

Women aged 18-43 years attending Sivas Cumhuriyet University Faculty of Medicine Hospital were included. The study population consisted of 30 women diagnosed with PCOS according to ESHRE/ASRM criteria and 30 healthy women with regular menstrual cycles who served as controls. All participants were non-obese (BMI \<30 kg/m²) and provided written informed consent.

Inclusion criteria

  • Women aged 18-43 years.
  • PCOS group: diagnosis of PCOS according to ESHRE/ASRM criteria, based on the presence of at least two of the following: oligo- and/or anovulation, clinical and/or biochemical hyperandrogenism, and polycystic ovarian morphology.
  • Control group: healthy women with regular menstrual cycles (21-35 days), modified Ferriman-Gallwey score \<8, and no unilateral or bilateral polycystic ovarian morphology on pelvic ultrasonography.
  • BMI \<30 kg/m².
  • No oral contraceptive use during the study period or within the previous 6 months.
  • Written informed consent.

Exclusion criteria

Exclusion Criteria:

  • Thyroid dysfunction, prolactinoma, Cushing disease, or late-onset congenital adrenal hyperplasia.
  • Diabetes mellitus, hypertension, dyslipidemia, coronary artery disease, or renal or hepatic dysfunction.
  • Additional gynecological disease.
  • Use of medications affecting sex hormone or carbohydrate metabolism.
  • Inadequate or unsuitable blood/serum sample for laboratory analysis.
05

Study design

Observational model
Case-control
Time perspective
Cross-sectional
Enrollment
60 participants (actual)
Patient registry
No
Biospecimen retention
Samples without dna

Groups and cohorts

  • PCOS Group

    Women aged 18-43 years diagnosed with polycystic ovary syndrome according to ESHRE/ASRM criteria (n=30).

  • Healthy Control Group

    Healthy women aged 18-43 years with regular menstrual cycles and without clinical or ultrasonographic features of PCOS (n=30).

06

What researchers measure

Primary outcomes

  1. Serum BRCC36 Level

    Serum BRCC36 levels measured using a commercially available human ELISA kit and compared between the PCOS and healthy control groups.

    Time frame: At study enrollment (single blood collection)

  2. Serum Telomerase Level

    Serum telomerase (TE) levels measured using a commercially available human ELISA kit and compared between the PCOS and healthy control groups.

    Time frame: At study enrollment (single blood collection)

07

Study locations

1 site
  • Sivas Cumhuriyet University
    Sivas, Sivas, Turkey (Türkiye)
08

References and documents

Individual participant data

Plan to share: No — maybe after de article submission i will plan to share.

No publications or documents are linked to this record.

09

Updates

1 registry update since Sep 25, 2026
Registered
First appeared on the registry. No changes since
Sep 30, 2026
Show all 1 update
  1. Sep 30, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07849166
Lead sponsor
Cumhuriyet University
Responsible party
Dilara Ulger Ozbek (Asistant Professor, Cumhuriyet University) — Principal investigator
First posted
Sep 30, 2026
Start date
Feb 20, 2024
Primary completion
Feb 20, 2025
Completion
May 1, 2026
Last update
Sep 30, 2026

Study contacts

Dilara Ülger Özbek, PhD
principal investigator · Cumhuriyet University

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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