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

M

Medical University of Graz

Status

Completed

Conditions

Type 1 Diabetes

Treatments

Device: Guardian RT
Procedure: Microdialysis
Device: Glucoday S

Study type

Observational

Funder types

Other

Identifiers

NCT00499954
CM9 diabetes_sensor

Details and patient eligibility

About

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.

Enrollment

16 patients

Sex

All

Ages

19 to 60 years old

Volunteers

No Healthy Volunteers

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

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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