- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06763380
Comparison of Ultrasound and Hysterosalpingography in Evaluation of Uterine Abnormality in Patients With Infertility
Comparison of Ultrasound and Hysterosalpingography in Evaluation of Uterine Abnormality in Patients With Primary and Secondary Infertility
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
To Compare diagnostic effectiveness of Ultrasound and Hysterosalpingography in detecting uterine abnormalities among Primary and Secondary Infertile women.
In order to obtain the necessary results, 73 patients were examined on Ultrasound and then referred for Hysterosalpingography at Radiology Department of Dr.Essa Lab and Punjab Radiology. Patients with Primary and secondary infertility between the age of 18 to 45 were included whereas pregnant women and women with PID and GTI were excluded. The data were collected utilizing the questionnaire and then processed in SPSS version 25.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
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Punjab
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Lahore, Punjab, Pakistan
- Dr. Essa Lab, High Q tower, Jail Road Lahore"
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- primary and secondary infertile women
Exclusion Criteria:
- Pregnant women. Women with PID
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
2D Ultrasound Scan
Time Frame: 12 Months
|
Uterine anomalies can be diagnosed on routine two-dimensional ultrasound scan
|
12 Months
|
|
Hysterosalpingography test
Time Frame: 12 Months
|
HSG is an x-ray exam of the uterus and fallopian tubes.
It uses a special form of x-ray called fluoroscopy and a contrast materia.
|
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
Additional Relevant MeSH Terms
Other Study ID Numbers
- MSAHS/Batch-Spring23/012
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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