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Comparing the usefulness of two types of masks used to provide breaths during general anaesthesia

Comparing the feasibility of ventilation with Novel nasal PAP device with conventional facemask in patients receiving general anaesthesia - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/11/077164
Enrollment
70
Registered
2024-11-21
Start date
Unknown
Completion date
Unknown
Last updated
2024-12-09

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: Novel Nasal PAP device: Novel nasal PAP device will be used to ventilate patients for about a minute under general anaesthesia and the parameters will be recorded every 15 seconds. Cont

Sponsors

AIIMSMangalagiri
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients of ASA I-III aged from 18 to 65 yrs are included in the study

Exclusion criteria

Exclusion criteria: Patients refusal Patients with anticipated difficult mask ventilation Patients with unanticipated difficult mask ventilation

Design outcomes

Primary

MeasureTime frame
•To measure delta Vt (difference between set tidal volume and delivered tidal volume) using both Super NO2VA and conventional face maskTimepoint: T0-Baseline(Post Induction) T1-15 secs T2-30 secs T3-45 secs T4-60 secs

Secondary

MeasureTime frame
•Change in the peak airway pressure (Paw) •Change in SpO2 •Measure EtCO2 values with both techniques •Grade the EtCO2 trace •Monitor the use of airway adjuncts •Agreeability between Super NO2VATM and conventional face mask Timepoint: T0-Baseline(Post Induction) T1-15 secs T2-30 secs T3-45 secs T4-60 secs

Countries

India

Contacts

Public ContactDr Muralidharan

All India Institute of Medical Sciences,Mangalagiri

dreeshwarmv@aiimsmangalagiri.edu.in9740122272

Outcome results

None listed

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