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A comparative study on two devices used to give breaths for general anesthesia in Keyhole abdominal surgeries.

A comparative study on use of Baska mask vs i-gel for general anesthesia in laparoscopic abdominal surgeries. - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/12/098276
Enrollment
70
Registered
2025-12-01
Start date
Unknown
Completion date
Unknown
Last updated
2025-12-08

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: Airway secured for general anesthesia in laparoscopic abdominal surgeries using Baska mask supraglottic airway device.: Patient airway is secured with appropriate sized Baska mask sup

Sponsors

Vinayaka Missions Kirupananda Variyar Medical College and Hospitals
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients undergoing laparoscopic abdominal surgeries under general anesthesia 2. Age group: 18 to 60 years 3. American Society of Anesthesiologists Physical Status (ASA-PS) I, II 4. Both male and female patients 5. Patient providing written informed consent

Exclusion criteria

Exclusion criteria: 1. Patient refusal or inability to provide informed consent 2. Age less than 18 or more than 60 years 3. American Society of Anesthesiologists Physical Status (ASA-PS) III or higher 4. Pediatric patients 5. Obstetric patients 6. Restricted mouth opening of less than 2.5cm 7. Patients at increased risk of aspiration of gastric contents (GERD, esophageal strictures, achalasia cardia, inadequate period of NPO etc.)

Design outcomes

Primary

MeasureTime frame
To study and compare first-time successful insertion rate and the ease of insertion.Timepoint: First-time successful insertion rate and the ease of insertion are assessed and recorded immediately (0 minutes).

Secondary

MeasureTime frame
To compare successful insertion time, leak fraction and the post operative laryngopharyngeal complications.Timepoint: Successful insertion time, leak fraction recorded immediately after device insertion(0 minutes) Post operative laryngopharyngeal complications recorded immediately after removing device, 2 hours, 12 hours post operatively.

Countries

India

Contacts

Public ContactDr Ajin Arul David

Vinayaka Missions Kirupananda Variyar Medical College and Hospitals

sabapathyv.appavoo@gmail.com9442566989

Outcome results

None listed

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