The Effect of Epidural Analgesia and Erector Spinae Plane Block on Intraoperative and Early Postoperative Outcomes in Open Gynecological Oncological Surgeries: a Prospective Randomized Study
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Analgesia
- Sponsor
- Duygu Akyol
- Enrollment
- 71
- Locations
- 1
- Primary Endpoint
- postoperative numerical rating scale
- Status
- Completed
- Last Updated
- 7 months ago
Overview
Brief Summary
The aim of this study is to compare the effectiveness of epidural block or erector spinae plane block applied for postoperative analgesia in gynecological cancer surgeries.
The main question(s) it aims to answer are:
[Is erector spinae plane block as effective as epidural block in postoperative analgesia?] The study was designed as a prospective randomized study. Researchers evaluated the effects of epidural block or erector spinae plane block applied for postoperative analgesia on pain scores, postoperative opioid use, and mobilization in patients undergoing gynecological cancer surgery.
Detailed Description
Our study was designed as a prospective randomized study. The investigators evaluated the analgesia methods used in patients undergoing surgery for gynecologic cancer between May 2024 and December 2024. The investigators evaluated the effect of epidural block or erector spina plan block on postoperative analgesia, opioid use and mobilization. Group 1: Epidural block group Group 2: Group with erector spina plan block
Investigators
Duygu Akyol
M.D
Bakirkoy Dr. Sadi Konuk Research and Training Hospital
Eligibility Criteria
Inclusion Criteria
- •Patients who will undergo open abdominal surgery
- •Patients with ASAII-III
- •Those between the ages of 30-70
- •Patients who are fully oriented and able to cooperate
Exclusion Criteria
- •Patients with ASAIV-V
- •Presence of active infection in the area where the block will be applied
- •Patients younger than 30 years old
- •Patients with BMI \> 40
- •Patients who are allergic to bupivacaine
- •Chronic analgesic use
Outcomes
Primary Outcomes
postoperative numerical rating scale
Time Frame: postoperatvely 24 hours
The primary purpose of this study is to compare NRS values at 0, 6, 12 and 24 hours in the first 24 hours postoperatively. Numeric rating scale was used to assess postoperative pain For example, 0-10 where 0 is no pain and 10 is the worst pain imaginable.
Secondary Outcomes
- Intraoperative amount of remifentanyl(intraoperative process)