Ignite Creation Date:
2024-05-06 @ 3:47 PM
Last Modification Date:
2024-10-26 @ 1:57 PM
Study NCT ID:
NCT04754893
Status:
COMPLETED
Last Update Posted:
2022-06-30
First Post:
2021-02-12
Brief Title:
Postbariatric EArly Discharge Controlled by Healthdot
Sponsor:
Philips Electronics Nederland BV acting through Philips CTO organization
Organization:
Philips Electronics Nederland BV acting through Philips CTO organization
Study Overview
Official Title:
Postbariatric EArly Discharge Controlled by Healthdot PEACH
Status:
COMPLETED
Status Verified Date:
2022-01
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:
PEACH
Brief Summary:
This clinical investigation is a single center patient preference trial in a tertiary hospital in the Netherlands designed to compare the outcome of two different recovery paths after standard of care bariatric surgery The difference between both recovery paths is that half of the patients will get the standard of care by staying one night in the hospital before returning home group B while the other half will receive a Healthdot directly after surgery and leave the hospital on the same day evening group A 200 patients will be recruited and can choose whether they want to be assigned to the the regular recovery path or receive a Healthdot and leave the hospital on the same day If they have no preference they will be randomly assigned to one of the two groups Patients in the outpatient recovery group will wear the Healthdot for 7 days at home and vital signs heart rate and respiratory rate together with context data on activity and posture will be transmitted to the hospital to monitor recovery The study is mainly designed to investigate if the clinical outcome in both groups is equal non-inferiority based on a combined outcome measures like 30 days readmission rate and patient satisfaction
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