Effect of Opioid-Free Anesthesia (OFA) on Postoperative Pain and Perioperative Nausea and Vomiting in Elective Laparoscopic .

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-60
SponsorAssiut University

About this trial

1. To evaluate the efficacy of a standardized multimodal Opioid Sparing (OS) protocol versus conventional opioid-based analgesia in reducing acute postoperative 2. To quantify opioid consumption reduction achievable through OS strategies 3. To assess the impact of OS on hemodynamic parameters during critical surgical phases 4. To compare recovery metrics (PONV, bowel function, ambulation) 5. To evaluate the safety profile of OS anesthesia

Eligibility criteria

Qualifiers

Adults aged 18 to 60 years scheduled for elective laparoscopic cholecystectomy. Elective must be included in title.

ASA (American Society of Anesthesiologists) physical status I or II.

Body Mass Index (BMI) < 35 kg/m².

Disqualifiers

Chronic opioid use (>30 MME/day for >3 months).

Contraindications to study medications (e.g., severe hepatic impairment; allergy/contraindication to lidocaine, dexmedetomidine, ketamine, fentanyl, or NSAIDs).

Renal dysfunction (eGFR <60 mL/min/1.73 m²).

Significant cardiac conduction abnormalities.

Trial design

Treatments tested in this trial

  • opoid free anesthesia

Treatment groups

110 Participants
are divided into 2 treatment groups

Locations

This trial has no locations

Sponsors and collaborators