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OpenTrials
Completed

NCT Number: NCT01049152

Continuous Glucose Monitoring and Inflammation in Nondiabetic and Diabetic Patients Undergone Hemodialysis

Evaluation of different glycemic variations between the dialysis period and non-dialysis period in two groups: nondiabetic and diabetic patients undergone two different hemodialysis methods. Thirty-six patients, males and females, aged 50-80 years, with end stage renal disease (ESRD) will undergo hemodialysis and continuous glucose monitoring (CGM). The investigators will evaluate also inflammation markers before and after the different hemodialysis methods.

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Key information

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • patients with or without diabetes mellitus
  • ESRD
  • undergone hemodialysis
  • males and females aged 50-80

Exclusion criteria

  • tumors
  • chronic inflammation diseases
  • AMI
  • acute pulmonary diseases

Treatment and study plan

Continuous glucose monitoring (CGM)

Device

CGM allocated one time for 3 days

Primary outcomes

  1. -Hemodialysis tolerability -Hypoglycemia numbers -Hyperglycemia numbers -Inflammation markers

    Time frame: before and after each procedure

Secondary outcomes

  1. variations of glycemia during the night; insulin-sensitivity

    Time frame: at the beginning of the first hemodialysis and at the end of the second hemodialysis

Sponsors and collaborators

Lead sponsor

University of Pavia

Other

Registry information

Important dates

Study start
2009
Primary completion
2014
Study completion
2014
First posted
Jan 14, 2010
Registry last updated
May 24, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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