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EOIPB in Laparoscopic Cholecystectomy: Impact on Opioid Consumption Guided by ANI and Analgesia Quality

S

Samsun University

Status

Completed

Conditions

Laparoscopic Cholecystectomy Surgery
Pain Management

Treatments

Other: Group EOİPB

Study type

Interventional

Funder types

Other

Identifiers

NCT06869837
OMUKAEK 2024/269

Details and patient eligibility

About

The aim of the study was to evaluate the response of regional anesthesia to remifentanyl consumption in patients undergoing laparoscopic cholecystectomy surgery.

Full description

Routine anesthesia and analgesia protocol will be applied to all participants. The study aims to evaluate the remifentanyl consumption of the participants by dividing them into two groups as those with and without block and then performing their monitoring (pulse, mean arterial pressure with noninvasive measurement, oxygen saturation, Analgesia Nociception Index, Bispectral index). Remifentanil level will be adjusted according to the ANI value. The target is to keep the ANI between 50-70.

Enrollment

80 patients

Sex

All

Ages

18 to 70 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Participants who will undergo elective laparoscopic cholecystectomy surgery,
  • Age 18-70,
  • ASA I-II physical status,
  • Body mass index (BMI) < 35 kg/m²,
  • Participants who have written consent to participate in the study

Exclusion criteria

  • Participants with routine analgesic consumption,
  • Those with coagulopathy,
  • Those with a history of local anesthetic allergy,
  • Those with cardiac arrhythmia and pacemaker,
  • ASA III and above, Those with dementia

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

80 participants in 2 patient groups

Group EOİPB
Active Comparator group
Description:
Bilateral External oblique intercostal plane block will be applied 45 minutes before surgery.
Treatment:
Other: Group EOİPB
Group Control
No Intervention group
Description:
No intervention will be made in this group.

Trial contacts and locations

1

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Central trial contact

ESMA BAHSI; HALE K CELIK

Data sourced from clinicaltrials.gov

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