Influence of Oral Vitamin C Supplement on the Inflammation Status in Dialysis Patients

Sponsor
Peking University First Hospital (Other)
Overall Status
Completed
CT.gov ID
NCT01356433
Collaborator
(none)
128
1
2
10
12.8

Study Details

Study Description

Brief Summary

Subclinical inflammation is a common phenomenon in patients receiving maintenance hemodialysis (MHD). This is because various pro-inflammatory cytokines are promoted due to metabolic acidosis, volume overload, and / or non-sterile dialysate.

As important antioxidants, vitamin C was prominently consumed by oxidative stress and inflammation. So patients receiving dialysis therapy usually had a low plasma vitamin C level.

It was documented that inflammation was associated with increased risk of cardiovascular morbidity and mortality in patients on dialysis. But the relationship between plasma Vitamin C and each of inflammatory markers and prealbumin was lacking. Because vitamin C had anti-inflammation effect on behalf of its electron receiving ability, the investigators made a hypothesis that vitamin C supplementation can reduce inflammation status in patients on maintenance dialysis

Condition or Disease Intervention/Treatment Phase
  • Drug: oral vitamin C
  • Drug: oral vitamin C
Phase 4

Detailed Description

Objective A cross-over study is designed to elucidate if oral vitamin C supplementation can reduce inflammation status in maintenance dialysis patients with low vitamin C level and high CRP level.

Patients, Methods and Expected results Patients About 100 dialysis patients were recruited. Patients will be divided into two groups, and will be followed for at least 6 months.

Methods Arm 1(50cases): is given oral vitamin C 200mg per day in the first 3 months, then stop oral VitC for the next 3 months.

Arm 2(50cases): is not given vitamin C in the first 3 months, then switch to receive oral VitC 200mg per day in the next 3 months.

The demographics were recorded. Plasma Vitamin C was measured by high-performance liquid chromatography. Serum albumin, prealbumin, high-sensitivity C-reactive protein (hsCRP), ferritin, hemoglobin will be measured.

Expected results There may be positive effect of vitamin C supplementation on inflammation in maintenance dialysis patients with vitamin C deficiency and high CRP level.

Study Design

Study Type:
Interventional
Actual Enrollment :
128 participants
Allocation:
Randomized
Intervention Model:
Crossover Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Effect of Oral Vitamin C on The Inflammatory Biomarkers in Hemodialysis
Study Start Date :
Aug 1, 2011
Actual Primary Completion Date :
Jun 1, 2012
Actual Study Completion Date :
Jun 1, 2012

Arms and Interventions

Arm Intervention/Treatment
Other: arm1, vitamin C treated first

Arm 1(50cases): intervention with oral vitamin C 200mg per day in the first 3 months, then stop oral VitC for the next 3 months.

Drug: oral vitamin C
cross-over study,2 arms Arm 1(50cases): is given oral vitamin C 200mg per day in the first 3 months, then stop oral VitC for the next 3 months. Arm 2(50cases): is not given vitamin C in the first 3 months, then switch to receive oral VitC 200mg per day in the next 3 months.
Other Names:
  • ascorbic acid
  • Drug: oral vitamin C
    Arm 2(50cases): is not given vitamin C in the first 3 months, then switch to receive oral VitC 200mg per day in the next 3 months.
    Other Names:
  • ascorbic acid
  • Other: Arm 2 control first

    Drug: oral vitamin C
    cross-over study,2 arms Arm 1(50cases): is given oral vitamin C 200mg per day in the first 3 months, then stop oral VitC for the next 3 months. Arm 2(50cases): is not given vitamin C in the first 3 months, then switch to receive oral VitC 200mg per day in the next 3 months.
    Other Names:
  • ascorbic acid
  • Drug: oral vitamin C
    Arm 2(50cases): is not given vitamin C in the first 3 months, then switch to receive oral VitC 200mg per day in the next 3 months.
    Other Names:
  • ascorbic acid
  • Outcome Measures

    Primary Outcome Measures

    1. the level of hsCRP [6 months]

    Secondary Outcome Measures

    1. the level of prealbumin [6 months]

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 80 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • Patients receiving maintenance hemodialysis or continuous ambulatory peritoneal dialysis, and dialysis vintage more than 3 months

    • Patients aged between 18 and 80 years older

    • VitC < 4ug/ml and hsCRP > 3mg/L

    • for HD patients, Kt/V > 1.2 per session, at least 3 sessions per week, 4 hours per session

    • for PD patients, Kt/V > 1.7 per week

    • age and gender matched health control

    Exclusion Criteria:
    • Active autoimmune disease, malignancy, hepatitis

    • Positive HIV serology

    • Any kind of acute infection within one month, chronic infection

    • Currently using steroids or immune-suppressants

    • Pregnancy or breast feeding

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 hemodialysis center of Renal Division, Department of Medicine, Peking University First Hospital Beijing Beijing China 100034

    Sponsors and Collaborators

    • Peking University First Hospital

    Investigators

    • Study Director: Li Zuo, MD, Renal Division, Department of Medicine, Peking University First Hospital, Beijing, China

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Li Zuo, Renal Division, Department of Medicine, Peking University First Hospital, Peking University First Hospital
    ClinicalTrials.gov Identifier:
    NCT01356433
    Other Study ID Numbers:
    • d2a3scvr
    First Posted:
    May 19, 2011
    Last Update Posted:
    Sep 21, 2012
    Last Verified:
    Sep 1, 2012
    Keywords provided by Li Zuo, Renal Division, Department of Medicine, Peking University First Hospital, Peking University First Hospital
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Sep 21, 2012