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UnknownNCT05562206

CGMIS 48-hour Feasibility Study

A 48hr Study to Test Feasibility of the Pacific Diabetes Technologies Continuous Glucose Monitor Infusion Set (CGMIS) Sensing Interstitial Glucose Continuously in the Immediate Vicinity of SQ Insulin Delivery in Adults With T1 Diabetes

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
20 (estimated)
Sponsor
Pacific Diabetes Technologies · Industry
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Accepted

Summary

This is a single center, single arm non-randomized study of 48-hour CGMIS wear duration incorporating two meal-challenge tests to explore the performance of a single insertion combined glucose-sensing insulin delivery cannula.

Conditions

Interventions

TypeNameDescription
DEVICECGMIS (Continuous Glucose Monitoring Infusion Set)An integrated combination CGM/insulin infusion system

Timeline

Start date
2022-08-30
Primary completion
2022-10-01
Completion
2022-11-01
First posted
2022-09-30
Last updated
2022-09-30

Locations

1 site across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT05562206. Inclusion in this directory is not an endorsement.

CGMIS 48-hour Feasibility Study (NCT05562206) · Clinical Trials Directory