SMART TAVR: SMART Watch Facilitated Early Discharge in Patients Undergoing Transcatheter Aortic Valve Replacement

Status: Recruiting
Location: See location...
Intervention Type: Device
Study Type: Observational
SUMMARY

The purpose of this study is to observe conduction disturbance, daily activity level, heart rates, oxygen saturation in patients who underwent Transcatheter Aortic Valve Replacement (TAVR) and to evaluate the utility of the HUAWEI Watch (HUAWEI Technologies Co., Ltd., Shenzhen, China) for the potential early warning sign of changes in multiple biometric parameters including heart rate, rhythm, oxygen saturation, activity, and sleep in patients following TAVR. This will be evaluated in the context of a recently implemented early discharge protocol.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
View:

• At least 18 years old;

• Be willing and able to provide informed consent to participate in the study;

• Not share HUAWEI Watch, HUAWEI phone with anyone else;

• Patient has severe aortic stenosis with echocardiographically derived criteria: mean gradient \> 40mmHg or maximum velocity greater than 4.0 m/s or an initial aortic valve area of \< 1.0 cm2;

• Patient who undergoing elective transfemoral transcatheter aortic valve replacement.

Locations
Other Locations
China
Second Affiliated Hospital, School of Medicine, Zhejiang University
RECRUITING
Hangzhou
Contact Information
Primary
Jiaqi Fan, MD
fanjiaqi@zju.edu.cn
+86-15267029492
Backup
Xianbao Liu, MD, PhD
liuxb2009@hotmail.com
+86-13857173887
Time Frame
Start Date: 2020-07-15
Estimated Completion Date: 2031-07-01
Participants
Target number of participants: 100
Treatments
SMART watch
Medical records from patients aged 18 years or older undergoing Transcatheter Aortic Valve Replacement
Sponsors
Leads: Second Affiliated Hospital, School of Medicine, Zhejiang University

This content was sourced from clinicaltrials.gov