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Arabic SAMANTA Questionnaire for Heavy Menstrual Bleeding Diagnosis

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Study Aim

This study aims to observe how accurately the Arabic version of the SAMANTA Questionnaire diagnoses heavy menstrual bleeding in individuals experiencing this condition.

What is being collected

Data Collection

Collected at a single point in time - Cross-sectional
Who is being recruted

Urogenital Diseases+9

+ Genital Diseases

+ Female Urogenital Diseases and Pregnancy Complications

From 15 to 45 Years
+7 Eligibility Criteria
See all eligibility criteria
How is the trial designed

Case-Only

Examining characteristics of individuals with a disease in order to identify genetic or environmental factors contributing to the condition.
Observational
Study Start: December 2025
See protocol details

Summary

Principal SponsorAssiut University
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Study start date: December 1, 2025

Actual date on which the first participant was enrolled.

This study focuses on improving the diagnosis of heavy menstrual bleeding (HMB) among non-pregnant women of reproductive age in Arabic-speaking regions. HMB can significantly affect a woman's quality of life by causing excessive menstrual blood loss that interferes with physical, social, and emotional well-being. Despite its high prevalence, there are few culturally adapted tools to diagnose HMB accurately in these regions. This study aims to adapt and validate the Arabic version of the SAMANTA questionnaire, a tool that could help identify women experiencing HMB and assess its impact on their lives, thereby addressing an unmet need for effective screening methods in low-resource settings. Participants in this study will complete the Arabic version of the SAMANTA questionnaire, which seeks to identify individuals experiencing heavy menstrual bleeding and assess how it affects their daily lives. The study evaluates the accuracy of this questionnaire as a diagnostic tool by testing its reliability and validity. Unlike complex methods that measure menstrual blood loss in research settings, this questionnaire offers a simple, cost-effective way to screen for HMB and its effects. The results aim to provide a practical solution for early and accurate diagnosis, potentially improving the quality of life for women affected by this condition.

Official TitleEvaluating the Reliability and Validity of the Arabic Version of the SAMANTA Questionnaire: A Step Toward Improved Diagnosis of Heavy Menstrual Bleeding.
Principal SponsorAssiut University
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

120 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Case-only

These studies focus only on individuals who have a specific disease. Researchers examine patterns—often genetic or environmental—to uncover what might be linked to the condition.

Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

From 15 to 45 Years

Range of ages for which participants are eligible to join.

Healthy volunteers not allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

Urogenital DiseasesGenital DiseasesFemale Urogenital Diseases and Pregnancy ComplicationsGenital Diseases, FemaleHemorrhageMenorrhagiaMenstruation DisturbancesPathologic ProcessesPathological Conditions, Signs and SymptomsUterine DiseasesUterine HemorrhageFemale Urogenital Diseases

Criteria

2 inclusion criteria required to participate
women, from 15 to 45 years old

Reproductive age women

5 exclusion criteria prevent from participating
Women with mental illness, or inability to make decisions or follow instructions.

Women with amenorrhea.

Postmenopausal women.

Pregnant women.

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Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Study Objectives

Study Objectives

Primary Objectives

Study Centers

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