ISRCTN52414847
Completed
Not Applicable
The effect on HbA1c in patients with diabetes mellitus when receiving either intravenous or erythropoietin stimulating agent therapy: a prospective follow-up study
Hull and East Yorkshire Hospitals NHS Trust (UK)0 sites30 target enrollmentMay 12, 2010
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- Hull and East Yorkshire Hospitals NHS Trust (UK)
- Enrollment
- 30
- Status
- Completed
- Last Updated
- 11 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •1\. Patients with established chronic kidney disease (stage III \- IV) (estimated glomerular filtration rate \[eGFR] using Modification of Diet in Renal Disease \[MDRD] 15 \- 59 mL/min/1\.73 m^2\) who are to undergo iron and/or erythropoiesis stimulating agent (ESA) therapy
- •2\. Patients who have established diabetes mellitus \- both type I and II
- •3\. Patients with no prior diagnosis of diabetes mellitus (control group)
- •4\. Aged 18 to 80 years, either sex
Exclusion Criteria
- •1\. Patients who not have renal failure (CKD stage I and II)
- •2\. Patients who are unable or do not wish to give consent
- •3\. Patients with currently investigated for potential blood loss
- •4\. Patients with a haematological malignancy/haemolysis
- •5\. Patients with known haemaglobinopathy
- •6\. Patient with significant liver disease (prothrombin time \[PT] greater than 16\)
- •7\. Patients with a diagnosis of myeloma
- •8\. Patients with severe hyperparathyroidism (parathyroid hormone \[PTH] greater than 800 picograms/ml)
Outcomes
Primary Outcomes
Not specified
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