Evaluating the Non-Inferiority of Airmod to Capnostream™35

NACompletedINTERVENTIONAL
Enrollment

284

Participants

Timeline

Start Date

December 16, 2021

Primary Completion Date

September 27, 2022

Study Completion Date

September 1, 2023

Conditions
Respiratory Rate
Interventions
DEVICE

Airmod

Both of the respiratory rate monitor (including experimental and reference device) are installed on the enrolled patients. The practitioners can clearly read the result of both devices.

Trial Locations (3)

106

Cathay General Hospital, Taipei

237

En Chu Kong Hospital, New Taipei City

10491

MacKay Memorial Hospital, Taipei

All Listed Sponsors
collaborator

Elite BioMedical Consulting Inc.

INDUSTRY

lead

Heroic Faith Medical Science Co., Ltd.

INDUSTRY

NCT05263791 - Evaluating the Non-Inferiority of Airmod to Capnostream™35 | Biotech Hunter | Biotech Hunter