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Comparison of breathing/respiratory rates obtained from Raybaby and GE B30 patient monitor among adults in the ICU

Clinical pilot study to find agreement between the respiratory rates obtained by raybaby with HCGs respiration monitor equipment (GE B30 patient monitor)

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
CTRI
Registry ID
CTRI/2020/06/025886
Enrollment
100
Registered
2020-06-15
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

None listed

Interventions

None listed

Sponsors

RIoT Solutions Inc
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: General ICU patients

Exclusion criteria

Exclusion criteria: Patient with known lung issues

Design outcomes

Primary

MeasureTime frame
To check the agreement between the respiratory rates between the GE B30 and raybaby among adults, aging between 18 to 80 in the intensive care unit. Timepoint: Respiratory rates (parameter of evaluation) from both devices will be compared at time intervals from 5 seconds or more and will be assessed post completion of monitoring of respective patients, starting from a minimum of 4 hour. Observations will be compiled every 2 weeks.—

Secondary

MeasureTime frame
To obtain usable respiration data with an average of 20% conversion rate from 4 to 10 hours of monitoring patients at periodic intervals of 5 minutes. Timepoint: Respiratory rates (parameter of evaluation) from both devices will be compared at time intervals from 5 seconds or more and will be assessed post completion of monitoring of respective patients, starting from a minimum of 4 hours. Observations will be compiled every 2 weeks.—

Countries

India

Contacts

Public ContactAnjali Palliyil Rajan

rayIoT Solutions Inc

anjali.p@raybaby.us9673637572

Outcome results

None listed

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