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Emergence time in patients Sevoflurane vs Isoflurane

Emergence time in patients undergoing ambulatory brachytherapy under general anaesthesia with a supraglottic device: A non-inferiority randomised clinical trial comparing isoflurane with sevoflurane

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/11/047441
Enrollment
100
Registered
2022-11-18
Start date
Unknown
Completion date
Unknown
Last updated
2025-08-18

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: Isoflurane: Will receive isoflurane to maintain bis 40-60 and emergence time will be noted Control Intervention1: Sevoflurane: will receive sevoflurane to maintain bis 40-60 and emergen

Sponsors

PGIMER chandigarh
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: American Society of Anaesthesiologists physical status I /II/III Middle aged women, 45-65 years Patient willing to participate in the tri

Exclusion criteria

Exclusion criteria: Any contraindication to use of supraglottic airway device Renal dysfunction(Serum creatinine >1.2 mg/dl) Advanced liver disease (liver enzymes twice the normal range or higher) Cardiac dysfunction BMI = 35 H/o of chronic use of sedatives/narcotics.

Design outcomes

Primary

MeasureTime frame
Awakening timeTimepoint: time from the end of procedure to eye opening in response to voice

Secondary

MeasureTime frame
Time to remove the airway device Time to discharge from PACU (Modified aldrette score 9) Percentage change in hemodynamics during induction and maintenance Incidence of any adverse events. Consumption of inhalation agent. Timepoint: time from the end of procedure to removal of I-gel

Countries

India

Contacts

Public ContactRamya R

PGIMER, chandigarh

navin_amc@yahoo.com8872377925

Outcome results

None listed

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