Using Erector Spinae Plane Block for Pain Relief in Gallbladder Surgery
Effects of Preoperative and Postoperative Errector Spinal Plan (ESP) Block on Postoperative Analgesia Score, Hemodynamic Response and Patient Satisfaction in Patients Undergoing Laparoscopic Cholecystectomy Surgery
This study is testing if a special pain relief technique called the Erector Spinae Plane block can help people feel less pain after gallbladder surgery.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 60 (estimated) |
| Ages | 18 Years to 65 Years |
| Sex | All |
| Sponsor | Harran University Academic / other |
| Locations | 1 site (Şanlıurfa) |
| Trial ID | NCT06670313 on ClinicalTrials.gov |
What this trial studies
This study investigates the effectiveness of the Erector Spinae Plane (ESP) block in providing analgesia for patients undergoing laparoscopic cholecystectomy. The ESP block is a regional anesthesia technique that utilizes ultrasound guidance to deliver local anesthetic to the paraspinal region, aiming to reduce pain and improve patient satisfaction post-surgery. The procedure can be performed with minimal sedation and may involve a single injection or continuous infusion via catheter. The study will assess pain control, hemodynamic stability, and overall patient satisfaction following the surgery.
Who should consider this trial
Good fit: Ideal candidates are adults aged 18-65 with ASA physical status I-II who are scheduled for laparoscopic cholecystectomy.
Not a fit: Patients with a BMI over 30, those with contraindications for the ESP block, or those classified as ASA III-IV-V will not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could significantly enhance pain management and patient satisfaction after gallbladder surgery.
How similar studies have performed: Previous studies have shown promising results with the ESP block in various surgical settings, indicating potential for success in this application.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * According to the physical classification of the American Society of Anesthesiologists (ASA), ASA I-II group, * between the ages of 18-65, Exclusion Criteria: * Patients who do not want to participate in the study; * BMI \>30, * Patients with contraindications for ESP block, * Uncooperative patients, * Those with renal failure, * Those with hepatic failure and * ASA III-IV-V group patients
Where this trial is running
Şanlıurfa
- Veli Fahri Pehlivan — Şanlıurfa, Turkey (Recruiting)
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.