Using a nerve block to reduce pain after laparoscopic colon surgery
Ultrasound Guided Erector Spinae Plane Block Reduces Postoperative Pain Following Laparoscopic Colorectal Operation: A Randomized Controlled Study
NA · Gachon University Gil Medical Center · NCT04238780
This study tests if a special nerve block can help reduce pain and improve recovery for people aged 20 to 70 after laparoscopic colon surgery.
Quick facts
| Phase | NA |
|---|---|
| Study type | Interventional |
| Enrollment | 60 (estimated) |
| Ages | 20 Years to 70 Years |
| Sex | All |
| Sponsor | Gachon University Gil Medical Center (other) |
| Locations | 1 site (Incheon) |
| Trial ID | NCT04238780 on ClinicalTrials.gov |
What this trial studies
This study evaluates the effectiveness of an ultrasound-guided erector spinae plane block in reducing postoperative pain and improving recovery quality following laparoscopic colorectal surgery. Participants aged 20 to 70 with specific health criteria will receive this nerve block in addition to a patient-controlled intravenous fentanyl device. The study aims to determine if this approach can enhance pain management and recovery outcomes for patients undergoing this type of surgery.
Who should consider this trial
Good fit: Ideal candidates are adults aged 20 to 70 with an ASA physical status of 1 or 2 scheduled for laparoscopic colorectal surgery.
Not a fit: Patients with a sensitivity to local anesthetics, bleeding disorders, or those who are pregnant may not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could significantly reduce postoperative pain and improve recovery times for patients after laparoscopic colorectal surgery.
How similar studies have performed: Other studies have shown promising results with similar nerve block techniques for postoperative pain management, indicating a potential for success in this approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * aged between 20 and 70 years, with an American Society of Anesthesiologists physical status of 1 or 2, who were scheduled for laparoscopic colorectal operation Exclusion Criteria: * sensitivity to local anesthetic, bleeding disorders , receiving anticoagulant, body mass index (BMI) over 35/kg/m2 spine or chest wall deformity pregnancy tolerance to opioid analgesics inability to use patient-controlled analgesia (PCA)
Where this trial is running
Incheon
- Gachon University College of Medicine, Gil Hospital — Incheon, Korea, Republic of (RECRUITING)
Study contacts
- Study coordinator: jungju choi, nd,phd
- Email: jjchoi2@gilhospital.com
- Phone: 8232 460 3624
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions: Postoperative Pain