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Comparison of efficacy of ventilation between Ambu bag and Novel Resuscitator Automation system in intubated patients

Comparison of novel Resuscitator Automation System(IS) v/s Ambu bag as intermediate ventilation device in emergency medicine department :A randomized controlled trial. - NIL

Status
Active, not recruiting
Phases
Phase 1Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/04/065747
Enrollment
100
Registered
2024-04-16
Start date
Unknown
Completion date
Unknown
Last updated
2025-05-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: Z991- Dependence on respirator

Interventions

Intervention1: Novel Inspire Resuscitator: Mechanical ventilation in intubated patient for 1 hour using In-Spire Resuscitator.Assessing Spo2, tidal volumes and effort of breathing. Control Interventi

Sponsors

Sagar.Virapannavar
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Assessment and approval by site investigator and sponsor assignee,that patient is eligible candidate for this treatment and study. The patient attender has been informed of the nature of the study,agrees to its provisions and has provided written informed consent. Patients who require invasive ventilation .

Exclusion criteria

Exclusion criteria: Cardiac Arrest DNR Not giving Consent

Design outcomes

Primary

MeasureTime frame
Stabilize respiratory parameter in intubated patients by assessing Spo2 ,Tidal volumes and effort of breathing.Timepoint: 1. Baseline (Before intubation) 2. At 5 minutes,10 minutes,15 minutes,20 minutes,25 minutes ,30 minutes,35 minutes,40 minutes,45 minutes,50 minutes,55 minutes,60 minutes after intubation.

Secondary

MeasureTime frame
Ease of operation by health care workersTimepoint: 1 hour

Countries

India

Contacts

Public ContactDrSheetal B Hiregoudar

Karnataka Institution of Medical Sciences Hubballi

drmadhuri_kurdi@yahoo.com9449590556

Outcome results

None listed

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