Glandular Urethral DisassemblyNCT05913128
Comparison Between Glandular Urethral Disassembly Versus Tubularized Incised Plate for Primary Distal Hypospadius Repair
A study testing Glandular Urethral Disassembly technique in people with Glandular Urethral Disassembly and Tubularized Incised Plate, run by Benha University at 1 site in Egypt.
Trial summary
To compare Glandular Urethral Disassembly technique versus Tubularized Incised Plate technique for Primary Distal Hypospadius Repair Read more about this study
- Who is it for?
- Ages 6 months to 6 years, men onlyHealthy volunteers can take part
- Conditions the study is for
- Glandular Urethral Disassembly, Tubularized Incised Plate, Distal Hypospadius Repair
- What is being tested?
- Glandular Urethral Disassembly technique
- Type of treatment
- Surgery or procedure
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 86 participants
- Where
- 1 siteEgypt
- Study dates
- 30 Jul 2023to 30 Dec 2023
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 6 months to 6 years
- Men only
- Healthy volunteers accepted
- Child
Who may be able to join
- Primary Distal Hypospadius
Who cannot join
- secondary Distal Hypospadius Recurrent Hypospadius
Trial locations and contacts
1 site in 1 country.
About this study
Official title: 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
Read the detailed description
Aim of study to compare glandular Urethral Disassembly technique versus Tubularized Incised Plate technique for Primary Distal Hypospadius Repair
- Being tested
- Glandular Urethral Disassembly technique
- Keywords
- Glandular Urethral Disassembly, Tubularized Incised Plate, Distal Hypospadius
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Glandular Urethral Disassembly techniqueProcedure or surgery
Also called Tubularized Incised Plate technique
For Primary Distal Hypospadius Repair
| Study group | Role | What they receive |
|---|---|---|
| First arm | Active comparator | Glandular Urethral Disassembly technique Receives: Procedure: Glandular Urethral Disassembly technique |
| Second arm | Active comparator | Tubularized Incised Plate technique Receives: Procedure: Glandular Urethral Disassembly technique |
What is being measured
The primary outcome is the main question the study is designed to answer.
Hospital stay
Hospital stay will be recorded in days.
Measured: up to14 days
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted22 Jun 2023
- Study start30 Jul 2023
- Primary completion30 Nov 2023
- Study completion30 Dec 2023
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Glandular Urethral DisassemblyStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Model description
- Prospective randomized clinical trial
- Masking
- Single blind
- Who is masked
- Investigator
- Enrolment
- 86 participants (actual)
Sponsor and investigators
- Lead sponsor
- Benha University
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Ahmed Abou Elezz Abdel Fattah, Benha University
- Investigators
- Ahmed AE Abdel Fattah, PhD, Principal investigator, faculty of medicine
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT05913128
- Sponsor's protocol ID
- Rc 7-2-2023
- Status last verified
- Jul 2026
- First submitted
- 28 Mar 2023
- Last updated
- 20 Jul 2026
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
Study at a glance
From the registry record, last updated by the sponsor on 20 Jul 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Comparison Between Glandular Urethral Disassembly Technique Versus Tubularized Incised Plate Technique for Primary Distal Hypospadius Repair
- ClinicalTrials.gov ID
- NCT05913128
- Acronym / sponsor ID
- Rc 7-2-2023
- Keywords
- Glandular Urethral Disassembly, Tubularized Incised Plate, Distal Hypospadius
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 86 participants (actual)
- Lead sponsor
- Benha UniversityUniversity, hospital or other
- Study start
- 30 Jul 2023 (actual)
- Primary completion
- 30 Nov 2023 (actual)
- Study completion
- 30 Dec 2023 (actual)
- First posted
- 22 Jun 2023 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
To compare Glandular Urethral Disassembly technique versus Tubularized Incised Plate technique for Primary Distal Hypospadius Repair
Detailed description
Aim of study to compare glandular Urethral Disassembly technique versus Tubularized Incised Plate technique for Primary Distal Hypospadius Repair
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind (investigator)
- Number of arms
- 2
- Model description
- Prospective randomized clinical trial
| Arm | Type | Receives |
|---|---|---|
| First arm | Active comparator | Procedure: Glandular Urethral Disassembly techniqueGlandular Urethral Disassembly technique |
| Second arm | Active comparator | Procedure: Glandular Urethral Disassembly techniqueTubularized Incised Plate technique |
Who may qualify
- Ages
- 6 months to 6 years
- Sex
- Male only
- Healthy volunteers
- Accepted
- Age groups
- Child
Key inclusion criteria (1 listed)
- Primary Distal Hypospadius
Key exclusion criteria (1 listed)
- secondary Distal Hypospadius Recurrent Hypospadius
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Glandular Urethral Disassembly techniqueAlso: Tubularized Incised Plate techniqueFor Primary Distal Hypospadius Repair | Procedure or surgery | First arm, Second arm |
Primary outcome
Hospital stay
Time frame: up to14 days
Hospital stay will be recorded in days.
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 20 Jul 2026.
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Ahmed AE Abdel Fattah, PhD principal investigator
faculty of medicine
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Glandular Urethral Disassembly technique in people with Glandular Urethral Disassembly and Tubularized Incised Plate, run by Benha University at 1 site in Egypt.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 20 Jul 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Egypt. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Hospital stay (time frame: up to14 days). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 20 Jul 2026.