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To compare postoperative upper airway complications following use of baska mask v/s endotracheal intubation in gynaecological diagnostic laproscopic surgeries.

A randomised interventional study for comparison of postoperative upper airway complications following use of Baska mask versus Endotracheal Intubation in gynaecological diagnostic laproscopic surgeries at SMS Medical College ,jaipur.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/08/044775
Enrollment
90
Registered
2022-08-22
Start date
Unknown
Completion date
Unknown
Last updated
2022-10-17

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: 45 patients will receive general anaesthesia using Baska mask device: To determine the proportion of cases who developed postoperative cough, sorethroat and hoarseness of voice after us

Sponsors

Swai mansingh medical college and hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.ASA grade one and two 2.Weight thirty -sixty kg 3.Undergoing gynaecological diagnostic laproscopic surgeries under general anaesthesia 4.Mallampatti grade one and two

Exclusion criteria

Exclusion criteria: 1.Patients with anticipated difficult airway 2.Patients with preoperative sorethroat 3.Patient with increased risk of aspiration of gastric contents 4.Surgery time more than 2hours

Design outcomes

Primary

MeasureTime frame
Difference in proportion of cases who developed postoperative cough in both groupsTimepoint: At baseline,30 min, 1hr ,2 hr, 6 hr, 12 hr, 24 hr.

Secondary

MeasureTime frame
1.To determine the difference in postoperative hoarseness of voice and sorethroat 2.To determine the time required for insertion of both the devices 3.To determine postextubation adverse eventsTimepoint: 1.To determine the difference in postoperative hoarseness of voice and sorethroat at different time interval 2.To determine the difference in time required for insertion 3.To determine the adverse events from postextubation to till 24 hours

Countries

India

Contacts

Public ContactDr kiran bala

Swai mansingh medical college jaipur

chatterjeerama30@gmail.com9828622026

Outcome results

None listed

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