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use of remifentanil in day care srugeries

fast track anaesthesia with remifentanyl : A Prospective Study in Ambulatory Surgeries - NIL

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/11/096911
Enrollment
100
Registered
2025-11-04
Start date
Unknown
Completion date
Unknown
Last updated
2025-11-17

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: Remifentanil (group R): Remifentanil administered as: IV bolus: 1 µg/kg Continuous infusion: 0.1 µg /kg/min, May be combined with low-dose midazolam or propofol as needed Control Int

Sponsors

GCS MEDICAL COLLEGE HOSPITAL AND RESEARCH CENTRE
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Willing to give consent ASA Physical Status I or II Undergoing elective ambulatory surgery

Exclusion criteria

Exclusion criteria: Known opioid allergy ASA 3,4 Severe cardiopulmonary disease Pregnancy

Design outcomes

Primary

MeasureTime frame
To evaluate hemodynamic stability of remifentanil To evaluate analgesia and sedation of remifentanil patients undergoing ambulatory surgeries To assess the time to recovery and discharge readiness following remifentanil-Timepoint: at start of procedure, every 5,10,15 mins and then every 30 mins until end of procedure

Secondary

MeasureTime frame
To compare patient and surgeon satisfaction scores with remifentanil versus fentanyl To compare surgeon satisfaction scores with remifentanil versus fentanylTimepoint: at start of procedure, every 5,10,15 mins and then every 30 mins until end of procedure

Countries

India

Contacts

Public ContactDr Divya Kheskani

GCS Medical college Hospital and Research Centre Ahmedabad

divya.kheskani@gmail.com8980738209

Outcome results

None listed

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