← Back to Clinical Trials
Recruiting Phase 2, Phase 3 NCT06740903

Evaluating Perioperative Outcomes: Dexmedetomidine vs Lignocaine in Laparoscopic Chlolecystectomy

Trial Parameters

Condition Hemodynamics Instability
Sponsor Sahiwal medical college sahiwal
Study Type INTERVENTIONAL
Phase Phase 2, Phase 3
Enrollment 140
Sex ALL
Min Age 20 Years
Max Age 70 Years
Start Date 2024-08-06
Completion 2025-08-06
Interventions
inj. dexmedetomidine infusion @ 0.2-0.4 μg/kg/hinj. lignocaine infusion @1-2 mg/kg/h

Brief Summary

Nowadays laparoscopic surgery is the first choice for many surgeries. Such surgeries have revolutionized the surgical practice and has markedly reduced the incidence of intraoperative and postoperative complications. To minimize these side effects associated with the use of opioids, various methods have been adopted. Recently, different trials have highlighted the possible role of dexmedetomidine and lignocaine in providing postoperative analgesia and attenuating hemodynamic response. Literature showed conflicting results regarding both these drugs. So, we want to find the evidence for local setting. This Randomized Controlled Trial will be done at Department of Anesthesia, Sahiwal teaching hospital, Sahiwal for 12 months. Sample size of 140 cases; 70 cases in each group will be included through non-probability consecutive sampling. Then patients will be divided in two groups by using computer generated random number table. In group A, patients will be given dexmedetomidine infusion. In group B, patients will be given lignocaine infusion. All anesthesia procedures will be done by researcher. Heart rate and mean arterial pressure will be assessed before induction of anesthesia, after every 10 mins every 30 mins till completion of surgery. Total operative time will be noted. After procedure, patients will be assessed for postoperative pain score. when pain will be ≥4 on visual analogue scale rescue analgesia will be given and time will be noted. Total duration from time of surgery till need for rescue analgesia will be noted. Duration of postoperative analgesia opioid consumption /24 hrs.) will be presented by using mean± SD.

Eligibility Criteria

Inclusion Criteria: 1. Patients of age 20-70 years 2. Both gender 3. Laparoscopic cholecystectomy under general Anaesthesia 4. ASA I-II. Exclusion Criteria: * Emergency surgery * Patients with history of allergic reaction to trial drugs * Patients with cardiovascular disease, sickle cell disease, psychiatric disorder, peripheral vascular disease, and neurological diseases (on medical record) * Anemia * Patient on TCA or Beta blocker drugs. * Uncontrolled hypertension (P≥160/100 mmHg) * Uncontrolled diabetes mellitus * Obesity BMI \> 35

Related Trials