Ignite Creation Date:
2024-05-06 @ 5:50 PM
Last Modification Date:
2024-10-26 @ 2:36 PM
Study NCT ID:
NCT05445492
Status:
COMPLETED
Last Update Posted:
2024-06-12
First Post:
2022-06-30
Brief Title:
Respiration Validation for CPM Device
Sponsor:
Analog Device Inc
Organization:
Analog Device Inc
Study Overview
Official Title:
Clinical Validation Study for Noninvasive Cardiopulmonary Management Device
Status:
COMPLETED
Status Verified Date:
2024-05
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
This study is designed to be a clinical validation study to ready the CPM System for FDA 510k submission This study will be conducted as a prospective non-randomized The study is non-significant risk since the CPM Device is noninterventional and noninvasive The study is primarily designed to validate the accuracy of the respiration rate and the changes in relative tidal volume All participants will be fitted with both the CPM Device as well as reference devices capnography and ECG Participants will be randomized between 4 procedures A-D which will determine the order of 10 exercises Each exercise has about 2 minutes of device recording and two minutes of rest Each exercise contains two positions sitting up for one minute and lying down for one minute For some exercises the participant will be instructed to breathe at a certain rate assisted by a metronome For other exercises the participants will breathe at a normal rate but change how deep the are breathing For the last all capnography reference devices will be removed and an ECG reference device will be placed After exercise 18 the participant will have all devices removed and the study visit will terminate The participant will receive a safety follow-up call about 1 week after their visit
Detailed Description:
None
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
True
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
True
Is an FDA AA801 Violation?:
None