Comparison of postoperative recovery score using fentanyl and remifentanyl as analgesic in neurosurgical patients

A randomised controlled study on comparison of post operative recovery score using fentanyl and remifentanyl as analgesia in neurosurgical patients posted for surgery having intracranial space occupying lesion - Nil

Status

Active, not recruiting

Phases

Phase 3Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/11/077398

Enrollment

Registered

2024-11-27

Start date

Unknown

Completion date

Unknown

Last updated

2024-12-09

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

Conditions

Health Condition 1: - Health Condition 2: O- Medical and Surgical

Interventions

Intervention1: Remifentanyl: 0.06 micrograms/kg/minute remifentanyl intravenous infusion intraoperatively till 20 minutes before end of surgery Control Intervention1: Fentanyl: 1.0 micrograms/kg bolus

Eligibility

Inclusion criteria

Inclusion criteria: patients between 20-60 years undergoing surgery for intracranial space occupying lesion belonging to ASA I, II and III grades of of either sex will be included

Exclusion criteria

Exclusion criteria: known case of diabetes and hypertension on treatment patients with poor GCS patients in liver and renal failure patients with neuropathies patient refusing participation in study

Design outcomes

Primary

Measure	Time frame
postoperative pain scoreTimepoint: Baseline 10 minutes 20 minutes 40 minutes 1 hour 2 hour 4 hour	—

Secondary

Measure	Time frame
1.intra and postoperative complications 2.postoperative pain assessment 3.postoperative nausea and vomiting 4. postoperative hemodynamic instabilityTimepoint: 10minutes 20minutes 40minutes 1hour 2hour 4 hou	—

Countries

India

Contacts

Public ContactDr Ram Badan Ram

Institute of Medical Sciences

rambadan.vns@gmail.com9336910579

Outcome results

None listed

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