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Investigation of Correlation Between Concentrations of Glucose in Blood and Interstitial Fluid in Type 1 Diabetics

An Open, Mono-Centre Trial to Investigate the Correlation Between Concentrations of Glucose in Arterialized Venous Blood and Subcutaneous Interstitial Fluid Applying Different Extracorporeal Sensor Techniques in Type 1 Diabetics

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00499954
Enrollment
16
Registered
2007-07-12
Start date
2006-02-28
Completion date
Unknown
Last updated
2007-07-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Type 1 Diabetes

Keywords

microdialysis, subcutaneous adipose tissue, glucose sensor, glucose monitoring, type 1 diabetes, Guardian RT, Glucoday S

Brief summary

This is a mono-centre trial performed at the Center for Clinical Research at the Medical University Graz. There will be a screening information and a study visit.In the study visit arterialized venous blood glucose values will be monitored and subcutaneous sampling of interstitial fluid (ISF) with microdialysis for glucose determination will be performed. Additionally to the laboratory analysis of the subcutaneous glucose samples, the glucose will be measured with extracorporeal on-line sensors and two marketed devices (Guardian RT and Glucoday S).The study visit will last 30 hours starting with the insertion of microdialysis catheters in the abdominal subcutaneous tissue and the insertion of the catheters for the Glucoday S system and Guardian RT system. The primary hypothesis of the study is: Interstitial fluid glucose concentration profiles correlate to the arterialized venous blood glucose concentration profile in type 1 diabetic subjects.

Interventions

DEVICEGlucoday S
PROCEDUREMicrodialysis

Sponsors

Medical University of Graz
Lead SponsorOTHER

Study design

Observational model
DEFINED_POPULATION
Time perspective
OTHER

Eligibility

Sex/Gender
ALL
Age
19 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

* Signed informed consent obtained before any trial-related activities. * Skin fold thickness of minimally 5 mm * Age of patients in the range from 19 to 60 years. * Type 1 diabetes

Exclusion criteria

* Severe acute and/or chronic diseases * Mental incapacity, unwillingness or language barriers precluding adequate understanding or co-operation. * Taking of any vasoactive substances or anticoagulation medication. * Diseases of the skin which could interfere with application of the catheters * Pregnancy or breastfeeding

Countries

Austria

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026