- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05913128
Comparison Between Glandular Urethral Disassembly Versus Tubularized Incised Plate for Primary Distal Hypospadius Repair
June 17, 2023 updated by: Ahmed Abou Elezz Abdel Fattah, Benha University
Comparison Between Glandular Urethral Disassembly Technique Versus Tubularized Incised Plate Technique for Primary Distal Hypospadius Repair
To compare Glandular Urethral Disassembly technique versus Tubularized Incised Plate technique for Primary Distal Hypospadius Repair
Study Overview
Status
Recruiting
Intervention / Treatment
Detailed Description
Aim of study to compare glandular Urethral Disassembly technique versus Tubularized Incised Plate technique for Primary Distal Hypospadius Repair
Study Type
Interventional
Enrollment (Estimated)
86
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Ahmed AE Abdel Fattah, PhD
- Phone Number: 002 01228555403
- Email: ahmed.aboelezz@fmed.bu.edu.eg
Study Locations
-
-
Qalubia
-
Banhā, Qalubia, Egypt, 74111
- Recruiting
- Faculty of medicine
-
Contact:
- Ahmed AE Abdel Fattah, Lecturer
- Phone Number: 002 01228555403
- Email: ahmed.aboelezz@fmed.bu.edu.eg
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Primary Distal Hypospadius
Exclusion Criteria:
- secondary Distal Hypospadius Recurrent Hypospadius
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: First arm
Glandular Urethral Disassembly technique
|
For Primary Distal Hypospadius Repair
Other Names:
|
|
Active Comparator: Second arm
Tubularized Incised Plate technique
|
For Primary Distal Hypospadius Repair
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Hospital stay
Time Frame: up to14 days
|
Hospital stay will be recorded in days.
|
up to14 days
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Ahmed AE Abdel Fattah, PhD, Faculty of medicine
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Estimated)
July 30, 2023
Primary Completion (Estimated)
November 30, 2023
Study Completion (Estimated)
December 30, 2023
Study Registration Dates
First Submitted
March 28, 2023
First Submitted That Met QC Criteria
June 17, 2023
First Posted (Actual)
June 22, 2023
Study Record Updates
Last Update Posted (Actual)
June 22, 2023
Last Update Submitted That Met QC Criteria
June 17, 2023
Last Verified
June 1, 2023
More Information
Terms related to this study
Other Study ID Numbers
- Rc 7-2-2023
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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-
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National Cancer Institute (NCI)CompletedMetastatic Urethral Carcinoma | Stage III Bladder Urothelial Carcinoma AJCC v6 and v7 | Stage III Ureter Cancer AJCC v7 | Stage III Urethral Cancer AJCC v7 | Stage IV Bladder Urothelial Carcinoma AJCC v7 | Stage IV Ureter Cancer AJCC v7 | Stage IV Urethral Cancer AJCC v7 | Ureter Urothelial Carcinoma and other conditionsUnited States, Canada
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-
State University of New York - Upstate Medical...Unknown
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