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ACTIVE NOT RECRUITING
NCT06326281
NA

Postoperative Pain Management in Laparoscopic Cholecystectomies

Sponsor: Ankara City Hospital Bilkent

View on ClinicalTrials.gov

Summary

This study is to demonstrate the effectiveness of external oblique intercostal plane block, a new block method, in the treatment of postoperative pain occurring after laparoscopic cholecystectomy operations, which are frequently and widely performed today. It aims to add new applications to multimodal analgesia methods, which provide the greatest contribution to the early recovery process after surgery, and to contribute to the early recovery process by increasing patient satisfaction.

Official title: Comparison of External Oblique Intercostal Plane Block Oblique Subcostal Transversus Abdominis Plane Block and Local Anesthetic Infiltration Methods in Laparoscopic Cholecystectomies

Key Details

Gender

All

Age Range

18 Years - 65 Years

Study Type

INTERVENTIONAL

Enrollment

100

Start Date

2024-03-20

Completion Date

2024-10-20

Last Updated

2024-06-05

Healthy Volunteers

No

Interventions

PROCEDURE

unilateral external oblique intercostal plane block group

USG guided external oblique intercostal plane block will perform unilateral with Bupivacaine 25 patient included and patients were observed for pain for 24 hours

PROCEDURE

unilateral oblique subcostal transversus abdomınıs plane block group

USG guided oblique subcostal transversus abdomınıs plane block block will perform unilateral with Bupivacaine. 25 patient included and patients were observed for pain for 24 hours

PROCEDURE

Local anesthetic infiltration group

Bupivacaine infiltration will be performed to trocar insertion sites. 25 patient included and patients were observed for pain for 24 hours

DRUG

Control group

All patients were followed using a standardized postoperative analgesia protocol which includes tramadol patient controlled analgesia. Tramadol at a concentration of 5 mg/mL is included in our patient controlled analgesia protocol (total volume 100 mL.) patient controlled analgesias were set to no basal infusion and 10 mg bolus doses with a 20 min lock time 25 patient included and patients were observed for pain for 24 hours

Locations (1)

Ankara Bılkent City Hospital

Ankara, Turkey (Türkiye)