Status:

COMPLETED

Analgesia Management in Bariatric Surgery

Lead Sponsor:

Ondokuz Mayıs University

Conditions:

Morbid Obesity

Bariatric Surgery Candidate

Eligibility:

All Genders

18-65 years

Phase:

NA

Brief Summary

Following laparoscopic bariatric surgery, multimodal analgesia is recommended to avoid the adverse effects of opioids by reducing their use. Although lidocaine, ketamine, and dexmedetomidine have been...

Detailed Description

Patients will be divided into three groups. Group L: The patients will receive intravenous lidocaine (2 mg/kg/h) immediately after anesthesia induction. At the end of the surgery, the dose will be de...

Eligibility Criteria

Inclusion

  • Body mass index\>35 kg/m2
  • The American Society of Anaesthesiologists (ASA) physical status class II III
  • Patients who will undergo an elective laparoscopic sleeve gastrectomy (LSG)

Exclusion

  • refusal to participate
  • allergy to the study drugs
  • chronic kidney disease (creatinine\>150 μmol/L)
  • mental illness
  • liver, respiratory or oncological disease,
  • cardiac dysfunction (ejection fraction \<40%),
  • uncontrolled hypertension,
  • preoperative analgesic use,
  • chronic pain,
  • history of alcohol or drug addiction

Key Trial Info

Start Date :

April 8 2021

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

July 1 2021

Estimated Enrollment :

78 Patients enrolled

Trial Details

Trial ID

NCT04836819

Start Date

April 8 2021

End Date

July 1 2021

Last Update

July 2 2021

Active Locations (1)

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Ondokuz Mayis University

Samsun, Atakum, Turkey (Türkiye), 55270