Quality of Life in Normogonadotropic Anovulation

NCT ID: NCT06208995

Last Updated: 2024-07-30

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Total Enrollment

300 participants

Study Classification

OBSERVATIONAL

Study Start Date

2023-07-01

Study Completion Date

2024-12-30

Brief Summary

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Among the causes of ovulation disorders (group II of anovulation according to the World Health Organization classification), the dominant one is polycystic ovary syndrome (PCOS), and the remaining cases are classified as Hypothalamic-Pituitary-Ovarian Axis Dysfunction (HPOD). The exact etiology of both entities is unknown. To diagnose PCOS, the Rotterdam criteria must be met and other conditions that may cause hyperandrogenism or ovulation disorders must be excluded. PCOS is more often accompanied by other endocrine and metabolic disorders, such as obesity, dyslipidemia, hyperandrogenism, insulin resistance, diabetes, hyperprolactinemia and thyroid diseases, as well as infertility due to ovulation defect. These conditions not only significantly reduce quality of life (QoL), but also lead to an increased risk of cardiovascular disease, metabolic syndrome, adverse obstetric outcomes and an increased risk of endometrial cancer, further impairing QoL.

Detailed Description

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A prospective questionnaire study will be conducted regarding the quality of life among women undergoing hormonal diagnostics due to anovulation. The study will include women aged 18-45 with ovulation disorders: PCOS (arm 1) and HPOD (arm 2). The quality of life will be assessed using the self-assessment method using the SF-36 questionnaire (Short Form Health Survey). The questionnaire is intended for a subjective assessment of health status. It consists of 11 questions containing 36 statements that allow you to determine eight quality of life indicators, i.e.: physical functioning, role limitations due to physical health, role limitations due to emotional problems, energy/fatigue, emotional well-being, social functioning, pain, general health, health change.

The percentage score on a scale of 0-100% in each of the 8 life domains will be compared between both arms of the study.

Conditions

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Anovulation Irregular Menses

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Arm 1

Polycystic Ovary Syndrome (PCOS)

36-Item Short Form Survey Instrument (SF-36)

Intervention Type OTHER

Answering 36 questions in a quality-of-life survey (RAND 36-Item Health Survey 1.0): https://www.rand.org/health-care/surveys\_tools/mos/36-item-short-form/survey-instrument.html

Arm 2

Hypothalamic-Pituitary-Ovarian Axis Dysfunction

36-Item Short Form Survey Instrument (SF-36)

Intervention Type OTHER

Answering 36 questions in a quality-of-life survey (RAND 36-Item Health Survey 1.0): https://www.rand.org/health-care/surveys\_tools/mos/36-item-short-form/survey-instrument.html

Interventions

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36-Item Short Form Survey Instrument (SF-36)

Answering 36 questions in a quality-of-life survey (RAND 36-Item Health Survey 1.0): https://www.rand.org/health-care/surveys\_tools/mos/36-item-short-form/survey-instrument.html

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* menstrual cycle length \<21 days or \>35 days
* age 18-45 years

Exclusion Criteria

* previous ovarian surgery
Minimum Eligible Age

18 Years

Maximum Eligible Age

45 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Sponsors

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Jagiellonian University

OTHER

Sponsor Role lead

Responsible Party

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Iwona Magdalena Gawron

PhD, MD

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Robert Jach, Prof., PhD

Role: STUDY_CHAIR

Jagiellonian University

Locations

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Jagiellonian University Medical College

Krakow, , Poland

Site Status RECRUITING

Countries

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Poland

Central Contacts

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Iwona Gawron, PhD, MD

Role: CONTACT

+48 12 4248551

Facility Contacts

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Iwona Gawron, PhD, MD

Role: primary

+48 12 4248551

Other Identifiers

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118.6120.21.2023

Identifier Type: -

Identifier Source: org_study_id

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