- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06763393
Correlation Between Adnexal Masses and Endometrial Thickness Measured With Ultrasound in Adults Women
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Adnexal masses, including ovarian cysts and other abnormalities, are common gynecological findings, while endometrial thickness is a crucial indicator for assessing conditions like endometrial hyperplasia or malignancy.
By analyzing ultrasound data, this research aims to determine whether the presence, size, or characteristics of adnexal masses have a significant relationship with variations in endometrial thickness.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
Punjab
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Sadiqābād, Punjab, Pakistan
- Sadiqabad
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Adult women typically defined as those aged 18 and older.
- Women with diagnosed adnexal masses, which could be cysts, tumors, or other growths in the adnexa (ovaries and fallopian tubes).
Exclusion Criteria:
- Pregnant women might have different hormonal and physiological changes that can affect endometrial thickness and adnexal masses.
- Recent gynecological history.
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
ultrasound for Endometrial Thickness
Time Frame: 12 Months
|
Endometrial thickness is well assessed on MRI.
Measurement should be taken at a mid-sagittal slice, similar to the ultrasound assessment plane
|
12 Months
|
|
ultrasound radiopaedia for Adnexal Masses
Time Frame: 12 months
|
Ultrasound (US) is an imaging technology that uses high-frequency sound waves to characterize tissue.
It is a useful and flexible modality in medical imaging and often provides an additional or unique characterization of tissues
|
12 months
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- MSAHS/Batch-Spring23/036
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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