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A study comparing opioid free and opioid based anaesthesia for recovery and Pain control after Gynecological cancer surgery

Comparison Of Opioid Based And Opioid free Anaesthesia Technique For Recovery Profile And Postoperative Analgesia In Patient Undergoing Gynecological Malignancy Surgery - NIL

Status
Active, not recruiting
Phases
Phase 3Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/01/101040
Enrollment
80
Registered
2026-01-14
Start date
Unknown
Completion date
Unknown
Last updated
2026-02-02

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

Conditions

Health Condition 1: C57- Malignant neoplasm of other and unspecified female genital organs

Interventions

Intervention1: Remifentanil-based anaesthesia (IV remifentanil bolus 1.5 g/kg followed by infusion 0.2 0.24 g/kg/min, titrated to SBP 20% of baseline): Group 1: Remifentanil) Induction with propofo

Sponsors

Self
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: INCLUSION CRITERIA : Patient giving consent to involve in study Patient posted for elective gynaecological malignancy surgery needing general anaesthesia Patient aged between 18-65 years Patient with American Society of anaesthesiologists (ASA) Class 1 to Class 2

Exclusion criteria

Exclusion criteria: BMI >35 kg/m2 Uncontrolled comorbidities viz. diabetes, hypothyroidism, hypertension etc. H/O Cerebrovascular disease Patient with known or newly diagnosed coagulopathy Patient allergic to study drugs Patient with american society of anesthesiology (ASA) classification 3 or more Those schduled for undergoing emergency surgery.

Design outcomes

Primary

MeasureTime frame
Primary objectives :To Assess total post operative analgesic consumption in 24 hours and time to first analgesic in opioid based and opioid free group.Timepoint: Just before induction (baseline) 5 minutes after induction 10 minutes after induction 15 minutes after induction 30 minutes after induction 60 minutes after induction

Secondary

MeasureTime frame
Time to eye opening,extubation time & time to shifting to PACU NRS score at PACU admission Time to PACU discharge criteria (modified aldrete score ) Time to PACU discharge criteria (modified aldrete score) Incidence of complications.Timepoint: NRS pain score at PACU admission then every 15 minutes in PACU Time to PACU discharge measured as the duration from arrival in PACU until Modified Aldrete Score equal to or more than 9

Countries

India

Contacts

Public ContactDr Namita Gupta

Mahatma Gandhi Medical college and Hospital

hardiktaneja99@gmail.com9896456466

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 7, 2026