Erectile dysfunction. Disorder of penis, unspecified
Conditions
Interventions
Intervention 1: Intervention group: Intervention group: Urological patients who will undergo endoscopic surgery will first undergo spinal anesthesia with Bupivacaine 0.25% and then sedation with Propo
Sponsors
Shahid Beheshti University of Medical Sciences
Eligibility
Sex/Gender
Male
Age
18 Years to 60 Years
Inclusion criteria
Inclusion criteria: Endoscopic Surgery Patients between 18 and 60 years
Exclusion criteria
Exclusion criteria: Surgeries that Affect Patient's Sexual Function. Allergy to Local Anesthetics Obligation to Change to Open Surgery Patient Refusal for spinal anesthesia
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Changes in the length of the penis and the erectile function. Timepoint: Penis length will be assessed before surgery, two weeks postoperatively, and three months postoperatively. The patient's erectile status will also be assessed before surgery, two weeks after surgery and three months after surgery. Method of measurement: The length of the penis will be measured by measuring the length of the penis in an elongated position with the help of a ruler. Patients' erectile status will also be assessed using the IIEF5 questionnaire. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactHouman teymourian
Shahid Beheshti University of Medical Sciences
Outcome results
None listed