Overview

Effects of Carnitine on Oxidative Stress to IVIR Administration to CKD Patients:Impact of Haptoglobin Genotype

Status:
Unknown status
Trial end date:
1969-12-31
Target enrollment:
0
Participant gender:
All
Summary
Anemia is a common disorder in CKD patients. It is largely attributed to decreased erythropoietin (EPO) production and iron deficiency. Therefore, besides EPO, therapy includes iron replenishment. However, the latter induces oxidative stress. Haptoglobin (Hp) protein is the main line of defense against the oxidative effects of Hemoglobin/Iron. There are 3 genotypes: 1-1, 2-1 and 2-2. Hp 2-2 protein is inferior to Hp 1-1 as antioxidant. So far, there is no evidence whether haptoglobin genotype affects iron-induced oxidative stress in CKD patients. In this proposed study we wished to examine whether Hp genotype influences intravenous iron administration (IVIR)-induced oxidative stress in CKD patients, and its impact on the response of these patients to L-Carnitine therapy.
Phase:
N/A
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
The Nazareth Hospital, Israel
Treatments:
Ferric gluconate
Criteria
Inclusion Criteria:

1. Patients that have been diagnosed as suffering from chronic kidney diseases at stages
3-4 and confirmed by MDRD.

2. CKD patients with Hb of less than 10 g%.

3. At age ≥18 y.

Exclusion Criteria:

1. Pregnant women.

2. Patient with CKD stage 5 on Dialysis.

3. Patients with severe liver diseases.

4. Patients with severe CHF.

5. Inter-current illness such as fever.

6. Allergic rhinitis.