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Comparison of Spinal Anesthesia and Spermatic Cord Block for Bilateral Orchiectomy

NCT06313775 · Status: ENROLLING_BY_INVITATION · Phase: NA · Type: INTERVENTIONAL · Enrollment: 18

Last updated 2024-03-15

No results posted yet for this study

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.

Conditions

  • Orchiectomy
  • Spermatic Cord Block
  • Spinal Anesthesia
  • Pain Score
  • Prostate Cancer

Interventions

PROCEDURE

bilateral orchiectomy

Bilateral simple orchiectomy is the surgical removal of both testicles through an incision in the scrotum.

Sponsors & Collaborators

  • Sanpasitthiprasong Hospital

    lead OTHER_GOV

Principal Investigators

  • Thararat Wanthawong, MD · Sanpasitthiprasong Hospital

  • Wattanachai Ungjaroenwathana, MD · Sanpasitthiprasong Hospital

  • Sahachart Atichosakun, MD · Sanpasitthiprasong Hospital

  • Rawisara Hongkrisadakorn, MD · Sanpasitthiprasong Hospital

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Sex
MALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2024-06-01
Primary Completion
2024-12-31
Completion
2024-12-31

Countries

  • Thailand

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06313775 on ClinicalTrials.gov