Ignite Creation Date:
2024-05-06 @ 8:27 PM
Last Modification Date:
2024-10-26 @ 3:27 PM
Study NCT ID:
NCT06383000
Status:
NOT_YET_RECRUITING
Last Update Posted:
2024-04-25
First Post:
2024-04-22
Brief Title:
Assessment of Effectiveness of Continuous Non-invasive Haemodynamic Monitor by Compared to Invasive Blood Pressure and Pulse Oximeter Monitoring on Patients Undergoing General Anesthesia Surgeries for More Than 60 Minutes
Sponsor:
BLZ Technology Wuhan CoLtd
Organization:
BLZ Technology Wuhan CoLtd
Study Overview
Official Title:
Assessment of the Effectiveness of the Continuous Non-invasive Haemodynamic Monitor
Status:
NOT_YET_RECRUITING
Status Verified Date:
2024-04
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:
The goal of this observational study is to assess whether the continuous non-invasive haemodynamic monitor MOH200 measuring blood pressure as well as pulse rate is effective or not in people undergoing general anesthetic surgeries for more than 60 minutes with planned invasive blood pressure and pulse oximeter monitoring
Researchers will compare blood pressure data derived from MOH200 to the invasive blood pressure IBP data to see if the MOH200 is effective to measure the blood pressure of a surgical person Also researchers will compare pulse rate data drived from MOH200 to that from the pulse oximeter to see if the MOH200 is effective to measure the pulse rate of a surgical person
Participants will be asked to be applied with MOH200 monitoring while IBP monitoring and pulse oximeter are applied And after 30 minutes of the surgery researchers will monitor the adverse effects occurred on the skin of participants to assess the safety of MOH200
Researchers will compare blood pressure data derived from MOH200 to the invasive blood pressure IBP data to see if the MOH200 is effective to measure the blood pressure of a surgical person Also researchers will compare pulse rate data drived from MOH200 to that from the pulse oximeter to see if the MOH200 is effective to measure the pulse rate of a surgical person
Participants will be asked to be applied with MOH200 monitoring while IBP monitoring and pulse oximeter are applied And after 30 minutes of the surgery researchers will monitor the adverse effects occurred on the skin of participants to assess the safety of MOH200
Detailed Description:
None
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None