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Minimally Invasive Scrotal Incision for Penile Prosthesis Implantation, Novel Technique.

Minimally Invasive Scrotal Incision for Penile Prosthesis Implantation, Novel Technique.

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05558163
Acronym
PPI
Enrollment
200
Registered
2022-09-28
Start date
2022-11-01
Completion date
2023-12-01
Last updated
2022-09-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Penile Prosthesis; Complications, Infection or Inflammation, Penile Prosthesis Infection

Keywords

erectyle dysfunction, penile prothesis

Brief summary

The main goals of this study are to examine the superiority of this novel technique and its acceptance by patients with ED candidate for PPI and compare these results with data available in the literature for ordinary peno-scrotal incision.

Detailed description

Rational for the expected superiority of scrotal approach over peno-scrotal approach in penile prosthesis implant (PPI): A- Expected to have all the previously mentioned pros of the traditional approach. B- Expected lower incidence of post-operative pain with our novel approach owing to lower sensitivity of scrotal skin and tension free wound closure compared to traditional peno-scrotal approach. C- Expected lower incidence of infection owing to multilevel wound closure done in our novel approach. D- Expected rapid wound closure and wound healing than traditional peno-scrotal approach owing to difference in embryologic origin of penile and scrotal skin. E- Validity of this novel approach for malleable and inflatable prosthesis implantation. F- Short learning curve owing to simplicity of the approach even for junior urologists. 3- Research methodology \- Responsible party: drmohamedalgammal@gmail.com Study Type: Interventional study Sampling: Hospital-based sample Estimated Enrollment: 200 participants Intervention Model: Patients who will undergo scrotal approach will be compared with a case-matched of patients who underwent PPI through peno-scrotal approach in our institution during the last 5 years. Study Start Date: 2022 Estimated Study Completion Date: 2023 Study Location: Al-Hussin and Sayed Galal, Al-Azhar University Hospital, Cairo, Egypt. Study Population: \- The study participants are male patients who are candidate for penile prosthesis implantation and will accept to do minimal scrotal incision procedure for treatment of ED. Study Sample: \- All available cases with complete medical record and accepted follow-up with us will be included. Pre-Operative Evaluation 1. Full medical history taking including full sexual history and (IIEF5) table 1. 2. Physical Examination including general, abdominal and local genital examination. 3. Laboratory investigations: 1. Complete urine analysis and urine culture 2. Blood chemistry tests include blood urea, serum creatinine, liver function tests, blood sugar, and coagulation profile. 3. Lipid profile. 4. Hormonal assessment including serum testosterone, Follicular stimulating hormone (FSH) Luteinizing hormone (LH) and prolactin. 5. Complete blood cell count (CBC). 6. Psychosexual assessment if needed. 4. Imaging: 1. Penile douplex Ultra-sonography. 2. Nocturnal penile tumescence and rigidity study, (NPTR or Rigiscan) if needed. 3. Abdomino-pelvic ultra-sonography with residual urine calculation. 4. Uroflowmetry if needed. 5. Cardiopulmonary assessment Post-operative evaluation: * Post-operative CBC. * Post-voiding residual urine volume. * (Qmax.) maximum flow rate. * Regular post-operative assessment of 1. Pain using Numeric Pain Rating Scale (NRS) 2. Wound healing, cosmetic appearance after healing and any incidence of infection. 3. Incidence of satisfaction after regaining sexual activity using SSI.

Interventions

PROCEDUREtransverse scrotal approach for PPI

penile prothesis implantation through penoscrotal approach outcome

PROCEDUREpenoscrotal approach for PPI

penile prothesis implantation through penoscrotal approach outcome

Sponsors

Al-Azhar University
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

Patients who will undergo scrotal approach will be compared with a case-matched of patients who underwent PPI through peno-scrotal approach in our institution during the last 5 years.

Eligibility

Sex/Gender
MALE
Age
30 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

The study participants are male patients who are candidate for penile prosthesis implantation and will accept to do minimal scrotal incision procedure for treatment of ED.

Exclusion criteria

* male patients with active scrotal infection. * contraindicaions to anasthesia.

Design outcomes

Primary

MeasureTime frameDescription
Subjective cure rate3 to 4 weakswill be judged according to rate of wound healing, cosmotic final results, scar tension and scar pain.
Objective cure rate4-12 weaksshould include rate of complications as fistula, scar, extensive fibrosis, infection rate, incidence of prosthetic removal.

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026