Ultrasound-guided Erector Spinae plane block versus Subcostal transversus Abdominis block for post operative pain relief in laparoscopic cholecystectomy.

Phase 4

Not yet recruiting

Conditions: Calculus of gallbladder without cholecystitis,

Registration Number: CTRI/2023/09/058005

Lead Sponsor: Maulana Azad Medical College and associated Lok Nayak Hospital

Brief Summary: We are comparing Erector Spinae Plane Block with Subcostal Transversus Abdominis Block for post operative analgesia in patients posted for Laparoscopic Cholecystectomy in Lok Nayak Hospital Delhi. A total of 40 patients with 20 patients in each group will be enrolled for the study. Patients will be explained about the study and written informed consent will be taken. We will be using standard general anesthesia for induction of the patients following which USG guided block site will be identified and local anesthetic drug will be administered. Patients will be followed up post operatively for 24 hours during which numerical rating scale for pain and time for first supplemental analgesia will determined. Overall patient satisfaction score will also be assesed .

Detailed Description: Not available

Recruitment & Eligibility

Status: Not Yet Recruiting

Sex: All

Target Recruitment: 40

Inclusion Criteria

1.18 to 60 years of age 2.American Society of Anesthesiologists Grade I and II.

Exclusion Criteria

1.Bleeding or Coagulation Abnormality 2.Local skin infection at the site of block 3.Pts on corticosteroids and immunosuppressive drugs 4.BMI >30 kg/mÂ² 5.Allergy to study medications 6.Inability to understand Numerical Rating Scale (NRS.

Study & Design

Study Type: Interventional

Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Time to request for first supplemental analgesia in post-operative period .	24 Hours

Secondary Outcome Measures

Name	Time	Method
1.Hemodynamic changes (Heart rate & mean arterial pressure) before induction(baseline), after induction, post block, at skin incision and for every 15 minutes intraoperatively.	2.Post-operative NRS score till 24 hours.

Trial Locations

Locations (1): Lok Nayak Hospital
🇮🇳
Central, DELHI, India
Lok Nayak Hospital
🇮🇳Central, DELHI, India
Dr Ankur Sharma
Principal investigator
8360971576
ankursharma99999@gmail.com