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Clinical Trial Summary

The goal of this randomized controlled trial is to compare intraoperative pain score, Morphine consumption during 6 and 12 hour after surgery, and postoperative complications between SA and SCB groups in metastatic prostate cancer patient. The main question it aims to answer are: • Is there a difference in the level of pain during bilateral orchiectomy between spinal anesthesia and spermatic cord block? Participants will undergo bilateral orchidectomy. They will be randomly assigned to two groups: the group receiving spinal anesthesia and the group receiving spermatic cord block If there is a comparison group: Researchers will compare intraoperative pain score, Morphine consumption during 6 and 12 hour after surgery, and postoperative complications in both groups of patients.


Clinical Trial Description

Objective : To compare intraoperative pain score, Morphine consumption during 6 and 12 hour after surgery, and postoperative complications between SA and SCB groups. Material and Method : This Randomized Controlled Trial that collected data from prostate cancer patients who underwent orchiectomy in our institution. Patients were randomly divided into two groups; SA and SCB. Data was collected on intraoperative pain score, 1 hour post-surgery, Morphine consumption during 6 and 12 hour after surgery and complications. All data was statistically analyzed using Independent t-test and Fisher's exact test. Inclusion criteria : Patients of all ages diagnosed with prostate cancer undergoing treatment with bilateral orchiectomy. Exclusion criteria : 1. Patients with a history of Xylocaine allergy. 2. Patients with uncorrected bleeding disorders. 3. Patients with paralysis or neurosensory deficits 4. Patients with dementia or cerebrovascular accidents (strokes) that impair communication. 5. Patients with contraindications for spinal anesthesia, including: - Patient refusal of spinal anesthesia. - Infection at the site of spinal injection. - Allergy to specific types of local anesthetics, such as Hyperbaric bupivacaine. - Inability of the patient to cooperate with the spinal anesthetic procedure. - Suspicion of high intracranial pressure based on abnormal physical examination. - Aortic stenosis with fixed cardiac output. - Low platelet count. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06313775
Study type Interventional
Source Sanpasitthiprasong Hospital
Contact
Status Enrolling by invitation
Phase N/A
Start date June 1, 2024
Completion date December 31, 2024

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