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Precision Pain Management vs. Routine Care in Laparoscopic Gallbladder Surgery

Efficacy Of Surgical Plethysmographic Index-guided Analgesia Versus Conventional Analgesia Technique In Laparoscopic Cholecystectomy Using Remifentanil - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/04/107527
Enrollment
184
Registered
2026-04-02
Start date
Unknown
Completion date
Unknown
Last updated
2026-04-27

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: Surgical plethysmographic index guided analgesia: Intraoperative remifentanil infusion titrated according to Surgical plethysmographic index monitoring to maintain SPI within target ran

Sponsors

Sir Ganga Ram Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Both males and females, aged 18-65 years ASA physical classification I to II

Exclusion criteria

Exclusion criteria: Known uncontrolled cardiovascular disease (e.g., hypertension, systolic and diastolic dysfunction) Liver function abnormality (liver enzymes more than 2 times the normal range) Kidney function abnormality (serum creatinine more than 1.4 mg/dl) Known psychiatric or neurological disorder Known uncontrolled endocrine disorder (diabetes mellitus, hypothyroidism) Known allergy or hypersensitivity to the study drug Recent intake of sedative medication or anti-psychotic medication Substance abuse Anticipated need for postoperative ventilation Refusal to informed consent

Design outcomes

Primary

MeasureTime frame
Intraoperative Remifentanil ConsumptionTimepoint: from induction of anaesthesia to competion of surgery

Secondary

MeasureTime frame
1. Postoperative pain (10-point NRS) during the first 24-hrs postoperative period 2. Postoperative nausea and vomiting (3-point PONV score) during the first 24-hrs postoperative period 3. Intraoperative haemodynamic instability (bradycardia/ tachycardia/ hypotension/ hypertension) Timepoint: immediately after shifting to recovery, 6 hours and 24 hours after recovery

Countries

India

Contacts

Public ContactDr Srishti

Sir Ganga Ram Hospital

ndua17@yahoo.co.in9313097996

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: May 1, 2026