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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05442541
Other study ID # 2021/514/216/15
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 1, 2022
Est. completion date February 1, 2022

Study information

Verified date June 2022
Source Dr. Lutfi Kirdar Kartal Training and Research Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

Women with endometriosis in our country and around the world face various difficulties during their menstrual periods in reproductive age. While some of these difficulties are caused by the environment, some of them are due to the insufficient development of personal consciousness. In our study, we aim to reveal the perspective of individuals and society on the menstrual period. Our primary aim in our study is to understand what kind of problems are experienced in different regions of our country during the menstrual period for women and how they are spent. Secondly, the effect of this period on women's quality of life will be examined.


Description:

Our research will be conducted between January 1, 2022, and February 1, 2022, in 7 different regions of our country, by asking questions to women of reproductive age from different groups. Each participant will be asked to answer the survey questions and the results will be analyzed. The survey will be done face to face. The questionnaire contains questions about women's socio-demographic data, their perspectives on their menstrual period, their information about endometriosis, and their perspectives on pads and birth control pills. Menstruating women of reproductive age between the ages of 18- 45 will be included in this study. As a result of the study, the problems experienced by women of reproductive age in different regions will be evaluated.


Recruitment information / eligibility

Status Completed
Enrollment 1829
Est. completion date February 1, 2022
Est. primary completion date February 1, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 45 Years
Eligibility Inclusion Criteria: - Menstruating women of reproductive age between the ages of 18- 45 will be included in this study. Exclusion Criteria: - Women with a history of hematological disease, cardiovascular disease, malignancy, advanced renal failure, active infection, diabetes mellitus, and pregnant women will not be included in the study.

Study Design


Intervention

Behavioral:
not included any interventions(Evaluation of menstrual well-being in women of reproductive age, field survey study)
This is a prospective cross-sectional analytical study conducted through a questionnaire.

Locations

Country Name City State
Turkey Kartal Dr. Lutfi Kirdar Research and Training Hospital Istanbul

Sponsors (3)

Lead Sponsor Collaborator
Dr. Lutfi Kirdar Kartal Training and Research Hospital IPSOS Group S.A, Turkish Endometriosis and Adenomyosis Society

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Disparities in menstrual hygiene and well-being between 7 regions of Turkey in women of reproductive age with a questionnaire In this study, the effect of the menstrual period on the quality of life of 1829 women living in seven different geographical regions of our country will be examined through a questionnaire. The goal of this study is to evaluate the menstrual well-being of women living in different regions of our country. 1 month
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