Viewing Study NCT07052292


Ignite Creation Date: 2025-12-24 @ 3:41 PM
Ignite Modification Date: 2025-12-29 @ 4:36 AM
Study NCT ID: NCT07052292
Status: ACTIVE_NOT_RECRUITING
Last Update Posted: 2025-12-04
First Post: 2025-06-26
Is Gene Therapy: True
Has Adverse Events: False

Brief Title: User Experience With DuraTouch® in Patients With Type 1 or Type 2 Diabetes
Sponsor: Novo Nordisk A/S
Organization:

Study Overview

Official Title: DuraTouch® - Post-Market Clinical Follow-up (PMCF) Study in a Real-world Setting
Status: ACTIVE_NOT_RECRUITING
Status Verified Date: 2025-11
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: This study looks at overall impact of the use of DuraTouch® in terms of ease, convenience to use and satisfaction in participants with either type 1 or type 2 diabetes.The study will last for about 12 weeks.
Detailed Description: None

Study Oversight

Has Oversight DMC: False
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: True
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?:

Secondary ID Infos

Secondary ID Type Domain Link View
U1111-1316-4217 OTHER World Health Organization (WHO) View