Who is sponsoring NCT05562011?

NCT05562011 is sponsored by Wake Forest University Health Sciences.

What condition does NCT05562011 study?

NCT05562011 studies Perioperative/Postoperative Complications.

What drugs are being tested in NCT05562011?

Interventions: Caretaker Device placement.

What is the status of NCT05562011?

NCT05562011 is currently TERMINATED.

Last reviewed 2023-12-20 · How we verify

Feasibility of a New Ambulatory Multi-vital Signs Monitor

NCT05562011 NA TERMINATED Results posted

The purpose of this research is evaluate vital signs (VS), which include non-invasive blood pressure, pulse rate, respiratory rate and Oxygen Saturation (SpO2) using a portable wrist monitoring device called a Caretaker. This device has been cleared by the Food and Drug Administration (FDA) for use and allows the study team to check vital signs in a participant's normal setting. Participation in this study will involve wearing this portable device at 2 different time points: 1. for up to 24 hours immediately during and after the participant's preoperative visit to obtain baseline vital signs during normal activity and during sleep and 2. after surgery up to 24 hours while participant recovers prior to discharge from the hospital

Details

Lead sponsor	Wake Forest University Health Sciences
Phase	NA
Status	TERMINATED
Enrolment	61
Start date	Wed Aug 18 2021 00:00:00 GMT+0000 (Coordinated Universal Time)
Completion	Mon Oct 24 2022 00:00:00 GMT+0000 (Coordinated Universal Time)

Conditions

Perioperative/Postoperative Complications

Interventions

Caretaker Device placement

Countries

United States