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Comparision of airway protector in laparoscopic surgery

Comparision of laryngeal mask airway proseal and laryngeal mask airway protector in laparoscopic surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2022/06/043562
Enrollment
120
Registered
2022-06-29
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: K806- Calculus of gallbladder and bile duct with cholecystitis Health Condition 2: K87- Disorders of gallbladder, biliarytract and pancreas in diseases classified elsewhere

Interventions

Intervention1: Nil: Nil

Sponsors

Department of Anaesthesiology
Lead Sponsor
Department of Anaesthesiology
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: Patients of either sex aged 18-60 years of ASA physical status I-II undergoing elective laparoscopic surgery

Exclusion criteria

Exclusion criteria: Patient having any of the following will be excluded from study Patients not giving written informed consent, Patients having anticipated difficult airway, Duration of surgery > 2 hours , Patient weight 100 kg, Any associated neurological disorders, gastrointestinal reflux disease, Body mass index �30kg/m2, Any contraindication to supraglottic airway devices, Inadequate fasting, full stomach.pregnancy,reactive airway disease etc.

Design outcomes

Secondary

MeasureTime frame
For this we will set intracuff pressure of LMA at 60 cm of H2O confirmed by manometer according to manufacturer�s recommendation. Now expiratory valve of circle system will be closed ,keep fresh gas flow at 3 L/min and stop the ventilationTimepoint: 24 hrs

Primary

MeasureTime frame
After completion of surgery device will be removed and patient will be shifted to postopearative recovery room. Two hours after surgery patient will be assessed for any airway morbidity by asking him like sore throat(constant pain), dysphonia(hoarseness) or dysphagia. Device will also be checked for any blood stain to asses any trauma during insertion .Timepoint: 48hrs to 72 hrs

Countries

India

Contacts

Public ContactProf BB Kushwaha

King Georges Medical University Lucknow

brij_kushwaha00634@yahoo.com9140398527

Outcome results

None listed

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