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Comparision Of Recovery Quality after giving Intravenous Lignocaine and Intravenous Fentanyl In Patients Undergoing Nasal Surgery Under General Anaesthesia

A Comparative Prospective Randomised Double blind Study To Compare Of Quality Of Recovery QoR 15 Following Administration Of Intravenous Lignocaine Versus Fentanyl In Patients Undergoing Functional Endoscopic Sinus Surgery Under General Anaesthesia In SMS Medical College Jaipur - Nil

Status
Active, not recruiting
Phases
Phase 3Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/04/085618
Enrollment
60
Registered
2025-04-25
Start date
Unknown
Completion date
Unknown
Last updated
2025-04-28

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

Conditions

Health Condition 1: J329- Chronic sinusitis, unspecified

Interventions

Intervention1: Intravenous Lignocaine Group: DOSE bolus of 1.5 mg per kg followed by infusion of 2 mg per kg hour ROUTE OF ADMINISTRATION Intravenous FREQUENCY OF ADMINISTRATION Single dose at ind

Sponsors

Department Of Anaesthesia Sawai Man Singh Medical College And Attached Hospital Jaipur
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Informed written consent Age 18 to 60 years Elective Functional Endoscopic Sinus Surgery under General anaesthesia ASA GRADE I AND II

Exclusion criteria

Exclusion criteria: Known hypersensitivity to local anaesthetics Body mass index greater than 30kg/m2 Patients with clinically significant neurological psychiatric or cardiovascular or renal and hepatic diseases History of alcoholic or drug abuse Patients who received an opioid medication within a 24 hour period before surgery

Design outcomes

Primary

MeasureTime frame
Quality of Recovery score QoR 15 postoperativelyTimepoint: At 24 hours

Secondary

MeasureTime frame
To Compare the postoperative analgesia duration and total number of doses in 24 hours between the two study groupsTimepoint: 24hours;To assess Numercal rating scale score at various time intervals between the two study groupsTimepoint: At 30mintes 6 hours 12 hours 24 hours;To compare the adverse effects between the two groups if anyTimepoint:

Countries

India

Contacts

Public ContactDr Potharlanka Jeevana

SMS MEDICAL COLLEGE AND ATTACHED HOSPITAL

aiims.priyanka@gmail.com9309482150

Outcome results

None listed

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