Retrospective Evaluation of Plane Blocks in Laparoscopic Cholecystectomy

Ultrasound-guided Oblique Subcostal Transversus Abdominis Plane Block Versus Serratus Intercostal Plane Block Plus Rectus Sheath Block; in Laparoscopic Cholecystectomy

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT03751540

Enrollment

Registered

2018-11-23

Start date

2018-05-01

Completion date

2018-11-26

Last updated

2018-11-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Postoperative Pain

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.

Interventions

PROCEDUREostap

this block is performed under general anesthesia in this patients for postoperative analgesia.

PROCEDURESIPB plus rectus sheath block

this block is performed under general anesthesia in this patients for postoperative analgesia.

Study design

Observational model

CASE_CONTROL

Time perspective

RETROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

18 Years to 80 Years

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

Design outcomes

Primary

Measure	Time frame	Description
opioid consumption	24 hours	Tramadol consumption in Patient Controlled Analgesia device and additional and rescue analgesic using

Secondary

Measure	Time frame	Description
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).

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026