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Anaesthesia for adults undergoing endoscopic nasal surgery

Surgical Field Conditions in Adults undergoing Functional Endoscopic Sinus Surgery under Propofol Total Intravenous Anaesthesia versus Sevoflurane General Anaesthesia: A Cohort Study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/02/049991
Enrollment
62
Registered
2023-02-22
Start date
Unknown
Completion date
Unknown
Last updated
2023-03-06

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: Propofol Group: Propofol Group (Group PR) â?? This group will be receiving Propofol both for induction at a dose of 1-2 mg/kg body weight(BW) and for maintenance of GA infusion at a rat

Sponsors

Sir Ganga Ram Hospital, New Delhi
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: BMIâ??18.5 â?? 24.9 kg/m2 ASA Grade â?? I and II

Exclusion criteria

Exclusion criteria: Inability to obtain informed consent ASA grade III and IV History of hypersensitivity to study agents or egg allergy Psychiatric illness Substance abuse Patient having any coagulopathy or hematological diseases Patient on anti-coagulant History of Covid-19 in the last 3 months Uncompensated systemic illness(cardiovascular, respiratory,endocrinologic)

Design outcomes

Primary

MeasureTime frame
Primary Outcome Measurement using Boezaart scale: No bleeding (cadaveric condition) Slight bleeding- no suctioning required Slight bleeding â??Occasional suctioning required Slight bleeding- frequent suctioning required;bleeding threatens surgical field a few seconds after suction is removed Moderate bleeding-frequent suctioning required and bleeding threatens surgical field directly after suction is removed Severe bleeding-constant suctioning required;bleeding appears faster than can be removed by suction;surgical field severely threatened and surgery usually not possibleTimepoint: At the end of surgery

Secondary

MeasureTime frame
Aonoâ??s scale Post-operative nausea and vomiting scoring systemTimepoint: till 24 hours postoperatively

Countries

India

Contacts

Public ContactDr Shashank Pandey

Sir Ganga Ram Hospital, New Delhi

shashankpandey16@gmail.com9811700660

Outcome results

None listed

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