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Effect of bag and mask ventilation with volatile anaesthetics after induction with thiopentone and vecuronium before intubation on postoperative nausea and vomiting in adult patients undergoing general anaesthesia via endotracheal tube.

Effect of mask ventilation with inhalational anaesthetics after induction with thiopentone and vecuronium before intubation on post operative nausea and vomiting in adult patients undergoing general endotracheal anaesthesia: a prospective randomized controlled study.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/04/051914
Enrollment
70
Registered
2023-04-24
Start date
Unknown
Completion date
Unknown
Last updated
2023-05-01

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: Endotracheal intubation: After induction with Thiopentone 5mg/kg body weight IV till the loss of eyelash reflexes. 0.1 mg/kg body weight of vecuronium IV will be administered to all pat

Sponsors

JSSAHER
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Adult patients of American Society of Anaesthesiologists (ASA) Physical status Class I and II, who will be scheduled to undergo elective surgery under general endotracheal anaesthesia and fulfilled the inclusion criteria mentioned hereafter, at JSS Medical College and Hospital, Mysore.

Exclusion criteria

Exclusion criteria: Patients with a history of motion sickness. Patients who are already on treatment with anti-emetics, a steroid medication, or any other drug known to cause emesis currently or in the immediate past. Patients with known hypersensitivity to isoflurane or thiopentone. Pregnant or nursing mothers. Patients with severe hepatic, renal, or cardiac diseases. Obese patients with BMI >30kg/m2. Patients with an anticipated difficult airways. Vomiting within 24 hours before surgery or of any organic etiology.

Design outcomes

Primary

MeasureTime frame
To assess the incidence of PONV during the first twenty-four hours (24 hours) after surgery. Severity of PONV, Number of rescue antiemetic medications required, Assessment of Apfel scoring, and comparison with the incidence and severity of PONV Timepoint: At immediate, 2, 4, 6, 12, 18, and 24 hours postoperative period.

Secondary

MeasureTime frame
The severity of PONV, Number of rescue antiemetic medications required, Assessment of Apfel scoring, and comparison with the incidence and severity of PONV Timepoint: At immediate, 2, 4, 6, 12, 18 and 24 hours post-operative period.

Countries

India

Contacts

Public ContactDR GURUDATT CL

JSS MEDICAL COLLEGE AND HOSPITAL

dattguru55@gmail.com9845312311

Outcome results

None listed

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