To assess the efficacy of a new device (RC device) in patients requiring ventilation in emergency department

To assess the efficacy of an automated AMBU bag operating (RC Device) device in patients requiring mechanical ventilation:a pilot study.

Status

Active, not recruiting

Phases

Phase 1

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2020/09/027819

Enrollment

Registered

2020-09-15

Start date

Unknown

Completion date

Unknown

Last updated

2023-01-09

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 Health Condition 2: J20-J22- Other acute lower respiratory infections

Interventions

Intervention1: RC device: the device will be attached to the patients in the emergency who require mechanical ventilation but cannot be shifted to ICU because of non availability of bed/ventilator Con

Eligibility

Inclusion criteria

Inclusion criteria: 1.Age group of 18-60 years 2.Any medical or surgical conditions requiring mechanical ventilation

Exclusion criteria

Exclusion criteria: 1.Age less than 18 years or greater than 60 2.Full blown ARDS 3.Severe emphysema/preexisting lung pathology 4.H/o Liver failure/Chronic kidney disease 5.Pregnancy

Design outcomes

Primary

Measure	Time frame
To assess the efficacy of an automated AMBU bag operating (RC Device) device in patients requiring mechanical ventilation.Timepoint: t1(baseline) when the machine is attached to the patient, t2 - 20 mins t3- 2 hrs t4 -4 hrs t5-8hrs t6-12hrs t7-16hrs t8-20hrs t9-24hrs	—

Secondary

Measure	Time frame
To assess the satisfaction score of care providerTimepoint: at 24 hours	—

Countries

India

Contacts

Public ContactRajeev Chauhan

PGIMER

dr.rajeevchauhan@gmail.com7087422950

Outcome results

None listed

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