Ignite Creation Date:
2024-05-06 @ 4:14 PM
Last Modification Date:
2024-10-26 @ 2:06 PM
Study NCT ID:
NCT04924569
Status:
RECRUITING
Last Update Posted:
2024-05-02
First Post:
2021-05-31
Brief Title:
Continence Care Registry
Sponsor:
Hollister Incorporated
Organization:
Hollister Incorporated
Study Overview
Official Title:
Continence Care Registry ConCaRe
Status:
RECRUITING
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:
ConCaRe
Brief Summary:
This observational research study aims to build a multinational electronic patient-reported outcomes ePRO registry of adult end users in outpatient and community settings using intermittent catheters to void via the urethra to manage urinary retention and incomplete bladder emptying Research participants will be asked to self-report on various attributes of their currently prescribed intermittent catheters and other various aspects of using an intermittent catheter
Detailed Description:
This observational research study aims to build a multinational ePRO registry of adult end users in outpatient and community settings using intermittent catheters to void via the urethra to manage urinary retention and incomplete bladder emptying Research resulting from data generated from an ePRO registry will factor in end user perspectives on intermittent catheterization habits and behaviors and intermittent catheter performance to inform and guide healthcare providers end users and caregivers in making the most informed healthcare decisions regarding intermittent catheterization Research participants will be asked to self-report on various attributes of their currently prescribed intermittent catheters and various aspects of habits and behaviors including health-related quality of life of using an intermittent catheter
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