About this trial
Open simple prostatectomy is still performed for selected patients with benign prostatic hyperplasia, particularly in cases with large prostate volume. Postoperative bleeding, hematuria, clot retention, and transfusion requirement are clinically important complications after this procedure.
This prospective randomized controlled trial will compare the effects of spinal anesthesia and general anesthesia on postoperative bleeding in patients undergoing open simple prostatectomy. Participants will be randomized into two groups: spinal anesthesia or general anesthesia. Tranexamic acid or any additional hemostatic agent will not be used. Postoperative bleeding will be assessed using hemoglobin and hematocrit changes, transfusion requirement, hematuria, clot retention, need for bladder irrigation, and bleeding-related reintervention.
The study aims to determine whether spinal anesthesia is associated with reduced postoperative bleeding compared with general anesthesia in open simple prostatectomy.
Eligibility criteria
Qualifiers
Male patients aged 18 years or older.
Diagnosis of benign prostatic hyperplasia (BPH).
Scheduled to undergo open simple prostatectomy.
American Society of Anesthesiologists (ASA) physical status I-III.
Disqualifiers
Refusal or inability to provide informed consent.
Patients scheduled for radical prostatectomy due to prostate cancer.
Emergency surgery.
Known coagulation disorders or clinically significant thrombocytopenia.
Trial design
Treatments tested in this trial
- Spinal anesthesia
- General anesthesia