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Clinical Trials/NCT07580807
NCT07580807CompletedNot Applicable

Penile Length After Spinal Anesthesia vs General Anesthesia for Cystoscope in Adults, Prospective Randomized Comparative Study

Tanta University1 site in 1 country200 target enrollmentStarted: March 1, 2025Last updated:
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Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
200
Locations
1
Study OverviewStudy DesignEligibility CriteriaInvestigatorsSitesRecords & IdentifiersSimilar Trials

Study Overview

Brief Summary

This research aimed to explore the impact of spinal and general anesthesia on penile length during surgery.

Detailed Description

Penile length and erectile function are complex physiological processes influenced by an interplay of neural, vascular, and hormonal factors. The process of penile erection involves the relaxation of smooth muscles in the corpora cavernosa, leading to increased blood flow and penile engorgement.

Erectile dysfunction (ED), a prevalent condition in men, has been associated with numerous risk factors such as age, cardiovascular disease, diabetes, and spinal cord injury.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
21 Years to — (Adult, Older Adult)
Sex
Male
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Adult male patients aged 21 years or older.
  • •Patients scheduled for elective urological surgeries including transurethral resection of the prostate (TURP) or transurethral resection of bladder tumor (TURT).
  • •Patients who provided written informed consent for participation in the study.

Exclusion Criteria

  • •Presence of a history of erectile dysfunction, penile deformities, or any urological conditions that could affect penile size.
  • •Undergoing emergency surgeries or procedures that required alternative anesthetic techniques.
  • •Known allergies or hypersensitivity to either spinal or general anesthesia.
  • •Inability or unwillingness to provide informed consent.

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Hossam Eldeen Osama Darwesh

Resident of Anesthesiology, Surgical Intensive Care and Pain Medicine, Tanta University, Tanta, Egypt.

Tanta University

Study Sites (1)

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