HIP: Effect of Hyperandrogenism on IVF Outcomes in PCOS Patients

Sponsor
Clinique Ovo (Industry)
Overall Status
Recruiting
CT.gov ID
NCT05555680
Collaborator
(none)
188
1
47.3
4

Study Details

Study Description

Brief Summary

Ovulatory dysfunction affects 18 to 25% of infertile women, the most common identifiable condition is polycystic ovarian syndrome (PCOS). The most frequent symptoms of PCOS are oligo-anovulation, hyperandrogenism and polycystic ovary appearance.

Hyperandrogenism is the main contributor that affects oocyte and embryo quality and decreases the success rates in PCOS patients undergoing IVF treatments.

The aim of this study is to determine the effect of hyperandrogenism as an independent factor on IVF success rates and oocyte/embryo quality in PCOS patients undergoing IVF.

Condition or Disease Intervention/Treatment Phase
  • Other: Ferriman-Gallwey Score

Detailed Description

Despite that PCOS patients obtain a higher yield of oocytes retrieved in IVF treatments, they often have lower fertilization, cleavage and implantation rates and a higher rate of miscarriage, which can be attributed to a poor quality of retrieved oocytes and the resulting embryos. Multiple studies compared IVF outcomes in PCOS patients to control groups and found that PCOS might negatively affect oocyte maturation rate, fertilization rate in conventional IVF and miscarriage rate. Hence, it seems that PCOS might be associated with poor outcomes in IVF cycles when compared to non-PCOS patients.

Study Design

Study Type:
Observational
Anticipated Enrollment :
188 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Effect of Hyperandrogenism on IVF Success Rates in PCOS Patients
Actual Study Start Date :
Jan 21, 2022
Anticipated Primary Completion Date :
Jan 31, 2025
Anticipated Study Completion Date :
Dec 30, 2025

Arms and Interventions

Arm Intervention/Treatment
PCOS patients with clinical or biochemical hyperandrogenism

Clinical hyperandrogenism consists of patients with one of the following conditions: Acne, Hirsutism (using modified Ferriman-Gallwey (FG) score) or Androgenic alopecia Biochemical hyperandrogenism consists of elevated serum level of at least one of the following hormones: Total testosterone, free testosterone, DHEAS, androstenedione using the cut-offs adopted by the laboratory.

Other: Ferriman-Gallwey Score
The Ferriman-Gallwey score is used to evaluate hirsutism. The examiner scores the subjects on a scale of 0-4 for terminal hair growth on eleven different body areas according to the Ferriman-Gallwey scoring system. A Ferriman-Gallwey score of 8 or more was considered diagnostic of hirsutism

PCOS patients with no clinical or biochemical hyperandrogenism

In this cohort, women have not be affected by either clinical of biochemical hyperandrogenism. The PCOS diagnosis will be based on oligo-anovulation and on polycystic ovaries during an ultrasound

Other: Ferriman-Gallwey Score
The Ferriman-Gallwey score is used to evaluate hirsutism. The examiner scores the subjects on a scale of 0-4 for terminal hair growth on eleven different body areas according to the Ferriman-Gallwey scoring system. A Ferriman-Gallwey score of 8 or more was considered diagnostic of hirsutism

Outcome Measures

Primary Outcome Measures

  1. Evaluate the effect of hyperandrogenism on frozen embryo transfer [10 days after frozen embryo transfer]

    Determine the effect of PCOS subjects affected by hyperandrogenism (HA) on clinical pregnancy rate following a frozen embryo transfer

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 39 Years
Sexes Eligible for Study:
Female
Inclusion Criteria:
  • Women between ages of 18 - 39 inclusively

  • ≥15 oocytes collected on the day of oocyte retrieval and/or anti-mullerian hormone (AMH) ≥ 4.0 ng/ml in the participant's medical chart in the last 24 months

Exclusion Criteria:
  • Male factor necessitating testicular sperm aspiration (TESA), testicular sperm extraction (TESE) or micro-TESE

  • Fertility preservation

  • Recurrent pregnancy losses (RPL) (defined as 2 or more failed clinical pregnancies as documented by ultrasonography or histopathologic examination,or 3 or more failed pregnancies before 14 weeks of gestation)

  • Oocyte donation

  • Medical diagnosis of non classic congenital adrenal hyperplasia diagnosed based on 17 hydroxyprogesterone level

Contacts and Locations

Locations

Site City State Country Postal Code
1 Clinique Ovo Montreal Quebec Canada H4P 2S4

Sponsors and Collaborators

  • Clinique Ovo

Investigators

  • Principal Investigator: Joanne Benoit, MD, Clinique Ovo

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Clinique Ovo
ClinicalTrials.gov Identifier:
NCT05555680
Other Study ID Numbers:
  • CCER 21-22 - 31
First Posted:
Sep 27, 2022
Last Update Posted:
Sep 27, 2022
Last Verified:
Sep 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Clinique Ovo
Additional relevant MeSH terms:

Study Results

No Results Posted as of Sep 27, 2022