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A study to compare lung ultrasound in detecting lung collapse (atelectasis) after general anaesthesia when using a breathing tube (endotracheal tube) versus a mask device (Proseal laryngeal mask airway)

Lung ultrasound guided evaluation of atelectasis after general anaesthesia using proseal laryngeal mask airway and endotracheal tube:a randomised controlled trial - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/09/094616
Enrollment
54
Registered
2025-09-11
Start date
Unknown
Completion date
Unknown
Last updated
2025-09-15

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

None listed

Sponsors

Maulana Azad Medical College and associated hospitals
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Age 18 -65 years with Physical status ASA I-III and BMI 19-30 kg/m? and Anticipated duration of surgery 30 minutes to 2 hours.

Exclusion criteria

Exclusion criteria: Difficulty in performing lung ultrasound - chest fractures, deformities or surgery, respiratory disease- chronic obstructive pulmonary disease, respiratory infections, smoking, h/o general anaesthesia or mechanical ventilation within the month preceding surgery, congestive heart failure, chronic renal insufficiency, liver cirrhosis, pregnancy, anticipated difficult airway and patients at risk of aspiration

Design outcomes

Primary

MeasureTime frame
Mean lung ultrasound scoresTimepoint: 30 min after removal of the airway device

Secondary

MeasureTime frame
Mean lung ultrasound scoreTimepoint: 15 min after securing the airway device and before device removal at the end of the surgery. ;SF ratio (SpO2/FiO2) ratioTimepoint: 15 min after securing the airway device, before device removal at the end of the surgery and 30 min after device removal. ;Lung dynamic compliance Timepoint: 15 min after securing the airway device and before device removal at the end of the surgery.;Incidence of postoperative pulmonary complicationsTimepoint: within 24 and 48 h post- surgery.

Countries

India

Contacts

Public ContactArohi Maheshwari

Maulana Azad Medical College

arohi.m.2510@gmail.com8290107955

Outcome results

None listed

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