Glucose in Dialysis Water in Non-diabetics

Sponsor
Regional Hospital Holstebro (Other)
Overall Status
Completed
CT.gov ID
NCT00439023
Collaborator
(none)
18
1
12
1.5

Study Details

Study Description

Brief Summary

The purposes are

  1. to measure the effect of dialysis with glucose on blood pressure, pulse rate, plasma concentration of glucose, plasma concentrations of glucagon, growth hormone, renin, angiotensin II, endothelin and body temperature, and

  2. to analysis the relationship between changes in blood pressure on the one hand and changes in vasoactive hormones on the other

Condition or Disease Intervention/Treatment Phase
  • Procedure: dialysis with glucose in dialysis water
Phase 4

Detailed Description

Measurement of hormones and blood pressure during dialysis treatment.

Study Design

Study Type:
Interventional
Actual Enrollment :
18 participants
Allocation:
Randomized
Intervention Model:
Crossover Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Effect of Glucose in Dialysis Water on Blood Pressure and Vasoactive Hormones in Dialysis Patients
Study Start Date :
May 1, 2006
Actual Study Completion Date :
May 1, 2007

Outcome Measures

Primary Outcome Measures

  1. Effect of glucose in dialysis water on blood pressure, insulin and vasoactive hormones [one week]

Secondary Outcome Measures

  1. Relationship between changes in blood pressure and changes in hormones during treatment [one week]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  1. Age > 18 years,

  2. Both men and women,

  3. Dialysis treatment for at least three months

Exclusion Criteria:
  1. Heart failure,

  2. Chronic liver disease,

  3. Diabetes mellitus,

  4. Malignant disease,

  5. Nephrotic syndrome,

  6. Lack of compliance, 7 Unwillingness to participate

Contacts and Locations

Locations

Site City State Country Postal Code
1 Holstebro Hospital Holstebro Denmark 7500

Sponsors and Collaborators

  • Regional Hospital Holstebro

Investigators

  • Study Chair: Erling B Pedersen, Professor, Regional Hospital Holstebro

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
, ,
ClinicalTrials.gov Identifier:
NCT00439023
Other Study ID Numbers:
  • MED.RES.2007.01.EBP
First Posted:
Feb 22, 2007
Last Update Posted:
Sep 15, 2015
Last Verified:
Sep 1, 2007
Keywords provided by , ,
Additional relevant MeSH terms:

Study Results

No Results Posted as of Sep 15, 2015