Comparison of the Effects of Moderate- and High-Dose Glucocorticoids on Postoperative Recovery

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-65
SponsorAnkara City Hospital Bilkent

About this trial

Laparoscopic cholecystectomy is a commonly performed minimally invasive surgical procedure; however, postoperative pain, nausea, and delayed recovery remain clinically relevant problems. Glucocorticoids such as dexamethasone are widely used in perioperative care for the prevention of postoperative nausea and vomiting and as part of multimodal analgesia strategies.

This prospective randomized controlled trial aims to compare the effects of moderate- and high-dose intravenous dexamethasone administered intraoperatively on postoperative recovery in patients undergoing elective laparoscopic cholecystectomy. The primary outcomes include postoperative nausea and vomiting, inflammatory markers (CRP and WBC), and Quality of Recovery-15 (QoR-15) scores. Secondary outcomes include postoperative pain scores, intraoperative remifentanil consumption, postoperative opioid consumption, and adverse events.

Eligibility criteria

Qualifiers

Age between 18 and 65 years

ASA physical status I-II

Scheduled for elective laparoscopic cholecystectomy

Undergoing general anesthesia

Disqualifiers

Patients younger than 18 years or older than 65 years

Known allergy to dexamethasone

ASA physical status III or higher

Surgical procedures lasting longer than 120 minutes

Trial design

Treatments tested in this trial

  • Saline (0.9% NaCl)
  • TAP Block
  • moderate dose Dexamethasone
  • High dose dexamethasone

Treatment groups

135 Participants
are divided into 3 treatment groups

Sponsors and collaborators