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Non Invasive End Tidal Carbon Dioxide Monitoring During Moderate Sedation

NCT04588272 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 120

Last updated 2022-03-18

No results posted yet for this study

Summary

CO2 monitoring through non-invasive methods at different O2 flow rates may provide an early warning sign of hypoventilation during procedural sedation.

Conditions

  • Carbon Dioxide

Interventions

DEVICE

DualGuard

DualGuard device (FlexiCare) which incorporate an endoscopy bite block with oxygen delivery and CO2 monitoring from both the mouth and nose simultaneously.

Sponsors & Collaborators

  • Assiut University

    lead OTHER

Principal Investigators

  • Mohamed Fathy · Assiut University

Eligibility

Min Age
20 Years
Max Age
60 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2020-06-01
Primary Completion
2021-12-01
Completion
2021-12-01

Countries

  • Egypt

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04588272 on ClinicalTrials.gov