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Clinical Trials in Turkey / NCT06606834
Starting soon Observational

Assessment of the Uterus Using Ultrasonographic Elastography in Women with Dysmenorrhea

NCT06606834 · tracked via the Priya Life Science Turkey tracker
Sponsor
Ufuk University
Phase
Observational
Started
2024-09-20
Last updated
2024-09-23

Condition(s) studied

Primary Dysmenorrhea

Investigational drug(s) / intervention(s)

sonoelastography

sonoelastography: Elasticity is defined as the ability of an organ or tissue to return to its original shape after being deformed by an applied force or stress. Based on this principle, sonoelastography is a technique used to assess the elasticity of tissues and organs during ultrasonography. This assessment allows measurement of changes in stiffness of soft tissues following physiological or pathological processes.

Study summary

The aim of this study is to perform sonoelastographic assessment of the uterus in patients diagnosed with primary dysmenorrhea and to compare these measurements with sonoelastographic evaluations of the uteri in asymptomatic individuals. This will enable, for the first time, the demonstration of whether the elasticity of the myometrial tissue contributes to the etiology of primary dysmenorrhea.

Secondary Objectives: To determine whether there is a correlation between the severity of primary dysmenorrhea and ultrasonographic markers.

Eligibility

Sex
FEMALE
Min age
18 Years
Max age
40 Years
Healthy volunteers
Accepted
Inclusion Criteria: 1. Women aged 18-40 years. 2. Women with primary dysmenorrhea who are willing to participate in the study. 3. Women without primary or secondary dysmenorrhea who agree to participate as a control group. Exclusion Criteria: 1. Women with secondary dysmenorrhea. 2. Patients with underlying uterine or adnexal pathologies (e.g., endometrial polyps, adenomyosis, uterine fibroids, adnexal masses, ovarian pathologies and cysts) identified via ultrasonography. 3. Individuals with a history of uterine surgery. 4. Individuals with a history of pelvic surgery. 5. Individuals who have delivered via normal spontaneous vaginal delivery or cesarean section.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Ufuk University Ankara Ankara

More Ufuk University trials in Turkey

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06606834 on ClinicalTrials.gov ↗ ← All trials in Turkey