- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04696874
Spectrum of Epididymis and Vas Deferens Anomalies Among Children With Cryptorchidism
Spectrum of Epididymis and Vas Deferens Anomalies Among Children With Cryptorchidism: A Retrospective Multi-center Study
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Background: Epididymal and vas deferens anomalies are not rare among children with cryptorchidism. They may affect fertility following orchiopexy.
Material and Methods: Data was collected retrospectively from six centers providing care for patients with undescended testicles from September 2017 to February 2019. All patients whose congenital anomalies of the epididymis or vas deferens were discovered incidentally during operative intervention for cryptorchidism and where photographs of the anomalies were taken were included.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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P.O.Pox. 11331
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Cairo, P.O.Pox. 11331, Egypt, Haddaek El-K
- Sarah Magdy Abdelmohsen
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- All included cases had photographic documentation.
Exclusion Criteria:
- cases without photographic documentation.
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
collection of cases
Time Frame: one and half year
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retrospective from multicenter university hospital
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one and half year
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Sarah M Abdelmohsen, MD, Aswan University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
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
- AswanUH1
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
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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