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Comparison of two airway securing devices in patients undergoing Cerebrospinal Fluid Diversion Surgery.

Comparison of Proseal Laryngeal Mask Airway and Endotracheal Intubation in Patients undergoing Ventriculo-Peritoneal Shunt Surgery: A Prospective Randomized Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/10/046878
Enrollment
50
Registered
2022-10-28
Start date
Unknown
Completion date
Unknown
Last updated
2022-11-21

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: Proseal Laryngeal Mask Airway: Proseal Laryngeal Mask Airway will be used in patients of group P to secure the airway and administer anaesthesia till the completion of surgery. Control

Sponsors

Post Graduate Institute of Medical Education and Research Chandigarh
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients aged 18 to 65 years, either gender 2. ASA I and II 3. Scheduled for VP shunt surgery under general anaesthesia will be included in the study.

Exclusion criteria

Exclusion criteria: 1. Patients refusal to participate in the study. 2. Features of acute raised intracranial pressure (bradycardia with hypertension, deranged neurological status, and active nausea and vomiting) 3. Patient with an anticipated difficult airway 4. ASA Physical Status III or IV 5. Body mass index >30 kgmâ??2 6. Upper respiratory tract infection 7. Increased risk of aspiration (unknown nil per os status, gastroesophageal reflux disorder, hiatus hernia, pregnancy, and diabetic patients) 8. Cervical spine fracture or instability

Design outcomes

Primary

MeasureTime frame
To compare the change in ONSDTimepoint: 5 minutes from baseline after securing the airway between both groups

Secondary

MeasureTime frame
â?¢ Comparison of the hemodynamic parameters (Heart rate, Mean arterial pressure, oxygen saturation) â?¢ Ventilation parameters like tidal volume (VT), respiratory rate (RR), and peak airway pressure. â?¢ Time taken and the number of attempts to secure the airway. â?¢ The surgeonâ??s and anesthesiologists satisfaction with techniques â?¢ Intraoperative and postoperative complications (within 24 hours). Timepoint: Intraoperative and up to 24 hours postoperative period

Countries

India

Contacts

Public ContactAmiya Kumar Barik

PGIMER Chandigarh

amiyabarik.scb@gmail.com08052919523

Outcome results

None listed

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