Retrospective Evaluation of Plane Blocks in Laparoscopic Cholecystectomy

Completed

• Conditions: Postoperative Pain
• Interventions: Procedure: ostap; Procedure: SIPB plus rectus sheath block

• Registration Number: NCT03751540
• Lead Sponsor: Maltepe University

Brief Summary

the investigators use usually a plane block for postoperative analgesia; if it suitable. İn laparoscopic patients; investigators used oblique subcostal transversus abdominis plane block; formerly. But in the last few months, the investigators have performed serratus intercostal (BRILMA) block with bilateral rectus sheath block. in this retrospective evaluation, the aim of the retrospective evaluation is to determine the effects of two block on postoperative opioid consumption.

Detailed Description

Not available

Study Timeline

• Study Start: 2018-05-01
• Status Verified: 2018-11
• Primary Completion: 2018-11-01
• Study First Submitted: 2018-11-19
• Study First Submitted QC: 2018-11-21
• Study First Posted: 2018-11-23
• Study Completion: 2018-11-26
• Last Update Submitted: 2018-11-26
• Last Update Posted: 2018-11-27

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 67

Inclusion Criteria

• patients undergoed laparoscopic cholecystectomy ASA I-II-III

Exclusion Criteria

• patients used another block or block combination
• no block performed patients
• procedure converted to open procedure

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Arm && Interventions

Group	Intervention	Description
OSTAP	ostap	Data of patients (performed oblique subcostal transversus abdominis plane-OSTAP- block for postoperative analgesia in laparoscopic cholecystectomy) will be collected.
SIPB plus rectus sheath block	SIPB plus rectus sheath block	Data of patients (performed serratus intercostal plane block-SIPB- plus rectus sheath block for postoperative analgesia in laparoscopic cholecystectomy) will be collected.

Primary Outcome Measures

Name	Time	Method
opioid consumption	24 hours	Tramadol consumption in Patient Controlled Analgesia device and additional and rescue analgesic using

Secondary Outcome Measures

Name	Time	Method
Pain assessed by NRS	24 hours	Changes in Numeric Rating Scale (NRS) at rest and on movement will be recorded at intervals. NRS is a unidimensional measure of pain intensity in adults. The NRS is a segmented numeric version of the visual analog scale (VAS) in which a respondent selects a whole number (0-10 integers) that best reflects the intensity of his/her pain. The 11-point numeric scale ranges from '0' representing one pain extreme (e.g. "no pain") to '10' representing the other pain extreme (e.g. "pain as bad as you can imagine" or "worst pain imaginable").

Trial Locations

Locations (1)

Maltepe University faculty of medicine; 🇹🇷 Istanbul, Turkey