Risks and Benefits of Scrotal Drainage in Penile Prosthesis Implant

Официальное название

Risks and Benefits of Using External Scrotal Drainage in Three-piece Penile Prosthesis Implant: a Prospective Randomized Study

Обзор

The goal of this prospective randomized study is to demonstrate if the use of an external scrotal drainage in penile prosthetic surgery can reduce the risk of post-operative complications without increase the risk of infections.

Подробное описание

After being informed about the study, all patients give writted informed consent. After that they will be randomized in two groups (A with drainage, B without drainage) using a random sequence generator. Then the patient will undergo the implantation of a three-component penile prosthesis following peri antibiotic prophylaxis with cephalosporins and aminoglycosides, the antibiotic prophylaxis will be continued on the first post-operative day surgery with a cephalosporin. In the group A it will be positioned at the scrotal level (using surgical access or using a second incision) an external drainage (10 Ch in aspiration) for 24 hours. The drainage will be removed on the first post-operative day. The degree of the hematoma will be determined using a 5-point Likert scales already approved in previous cases. Subsequently patients will carry out periodic check-ups at 7, 15 and 30 days after the operation to evaluate the appearance of hematomas and surgical site infection. After that, they will carry out check-ups every month for the first 3 months, then every 3 months for the first year and finally annually up to the fifth year after the intervention. During the clinical check-ups, it will also be defined the time of use of the penile prosthesis.

Вмешательства

• Устройство External scrotal drainage
  Application of external scrotal drainage during three-component penile prosthesis placement

Первичные конечные точки

• Post-operative infectious episodes [Срок оценки: One month]

Вторичные конечные точки (8)

• Post-surgical hematoma [Срок оценки: One month]
• Volume of drained material [Срок оценки: 24 hour]
• Manipulation of the activation pump [Срок оценки: Up to 12 weeks]
• Activation of the device [Срок оценки: Up to 12 weeks]
• Use of the penile prosthesis [Срок оценки: Up to 12 weeks]
• Effectiveness of external drainage in subgroups [Срок оценки: Up to 12 months]
• Effectiveness of external drainage in subgroups [Срок оценки: Up to 12 months]
• Effectiveness of external drainage in subgroups [Срок оценки: Up to 12 months]

Критерии участия

Критерии включения

• Written informed consent signed voluntarily according to the rules of good clinical practice (Declaration of Helsinki) and national regulations (Appendix B).
• Genetically male patient.
• Age ≥ 18 years.
• Patient suffering from ED of variable and/or multifactorial etiology.
• Patient suffering from ED not responsive to iPDE-5.
• Patient suffering from unresponsive or non-tolerant ED

Критерии исключения

• Absence of signed written informed consent (Appendix B).
• Age <18 years.
• Genetically female patients.
• Patient with active peno-scrotal infection.
• Patient with active systemic infection.
• Immunosuppressed patient.
• Patient with haematological pathologies that may cause an increased risk of bleeding.
• Patients suffering from Peyronie's Disease who must undergo simultaneous plaque surgery.
• Any condition or situation that, in the opinion of the investigator, places the patient at significant risk, may confound the results of the study, or significantly interfere with the patient's participation in the study.
• The patient declares that it will be impossible for him to participate in follow-up consultations.

Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.

Здоровые добровольцы: Нет

Дизайн исследования

Распределение

Рандомизированное

Модель

Параллельные группы

Маскирование

Открытое

Основная цель

Лечение

Центры проведения

Италия · 2 центра

• SCDU Urologia — Torino
• A.O.U. Città della Salute e della Scienza di Torino — Turin

Идентификаторы

NCT: NCT06147791 · 833.300

Первоисточники (государственные реестры)

• ClinicalTrials.gov (NIH, США)

Открыть это исследование на ClinicalTrials.gov ↗