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Comparison of the effects of two different General anaesthesia agents in adult patients undergoing General anaesthesia with airway Mask

A Cross Sectional Study Comparing the Effects of Sevoflurane and Desflurane in adults patients undergoing General Anesthesia with Laryngeal Mask Airway - not applicable

Status
Recruiting
Phases
Phase 4
Study type
Observational
Source
CTRI
Registry ID
CTRI/2025/09/094814
Enrollment
60
Registered
2025-09-15
Start date
Unknown
Completion date
Unknown
Last updated
2025-10-13

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: Group A patients for GA with Sevoflorane anesthesia through inhalational route: Thirty patients randomly selected by using a computer-generated random number for Group A will receive G

Sponsors

Department of Anesthesiology
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ASA physical status I and II Patients scheduled for elective surgery under GA with LMA Patient is willing to participate in the research

Exclusion criteria

Exclusion criteria: ASA physical status III and above Pregnant patients, paediatric patients Patient scheduled for emergency surgeries Patient with a history of smoking, chronic alcoholism, drug abuse, and psychiatric disorder Patient refusal

Design outcomes

Primary

MeasureTime frame
To observe and compare group A and B regarding the total volume of the inhalational agent, namely Sevoflurane or Desflurane used, total dose of the analgesic drug requirement, intraoperative hemodynamic stability, oxygen saturation, postoperative recovery score, and postoperative side effects, if any, will be assessed and documented for comparisonTimepoint: Before starting the procedure, the baseline parameters of vital signs, SpO2, Heart rate, blood pressure, ECG, and temperature will be assessed. After every 10 minutes till the end of the surgery duration of surgery post post-operative recovery score, and once the patient recovers from General anaesthesia, all these parameters will be assessed and compared between the two groups

Secondary

MeasureTime frame
Nausea, Vomiting, Sore throatTimepoint: Hourly for 4hrs then after 24hrs

Countries

India

Contacts

Public ContactDr B Kala

BIHER university

kalamhn@gmail.com9444680908

Outcome results

None listed

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