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A randomised study to compare the neuroendocrine and stress response markers in patients undergoing laparoscopic cholecystectomy under conventional general anaesthesia versus under opioid free anaesthesia

A randomized comparative study to evaluate inflammatory and neuroendocrine stress response markers in opioid free anaesthesia versus conventional anaesthesia technique for laparoscopic cholecystectomy - NIL

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/08/056206
Enrollment
40
Registered
2023-08-07
Start date
Unknown
Completion date
Unknown
Last updated
2023-08-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: Opioid Free Anaesthesia: Each patient will receive Ketamine 0.5 mg/kg at the time of induction of anaesthesia. Dexmedetomidine infusion will be prepared as 1μg/ml
after creation of pneumoperitoneum Dexmedetomidine infusion at the rate of 0.5ml/kg/hr (0.5μg/kg/hr) will be administered. Infusion will be stopped upon resection of the hall bladder. Single time inf

Sponsors

University College of Medical Sciences and Guru Tegh Bahadur Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients giving consent for the study and belonging to ASA grade I or II, scheduled for elective laparoscopic cholecystectomy under general anaesthesia.

Exclusion criteria

Exclusion criteria: 1. Patients with known cardiovascular, pulmonary, psychological or neurological diseases 2. Patients who have signs and symptoms of raised intracranial tension 3. Patients with known allergies to the study drugs 4. Obese patients (BMI > 30kg/m2)

Design outcomes

Primary

MeasureTime frame
Comparison of CRP values at 24 hours post induction in the two groupsTimepoint: 24 hours post induction

Secondary

MeasureTime frame
To compare in the two groups: Values at 6hrs post induction of various biochemical markers such as i) CRP ii) IL-6 iii) ESR iv) S. Cortisol v) S. Albumin vi) Blood Glucose Post-operative recovery using Modified Aldrete score Post-operative pain using Numeric Rating Scale (NRS) Total dose of rescue analgesia required in 24 hoursTimepoint: 6 & 24 hours post induction

Countries

India

Contacts

Public ContactDr Shubhang Singh

University College of Medical Sciences and Guru Tegh Bahadur Hospital

rudoc@rediffmail.com9871409907

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026