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临床试验/NCT01817699
NCT01817699终止4 期

A Factorial Randomized Controlled Trial of Correcting Anemia and Native Vitamin D Supplementation in Kidney Transplant Recipients

CANDLE-KIT Trial Study Group1 个研究点 分布在 1 个国家目标入组 161 人开始时间: 2013年4月1日最近更新:
适应症
干预措施

试验速览

阶段
4 期
状态
终止
发起方
入组人数
161
试验地点
1
主要终点
Change in allograft kidney function

研究概览

简要总结

The purpose of this study is to evaluate the effect of anemia correction and vitamin D supplementation in kidney transplant recipients.

详细描述

Sample size estimation:

The previous trial (the CAPRIT study) showed that 2.0 g/dL increase of hemoglobin (Hb) reduced 69% of 2-year decline in estimated glomerular filtration rate (eGFR) (Choukroun G, et al. J Am Soc Nephrol, 2012). Given that the annual eGFR decline in our patients with Hb level <10.5 g/dL was 1.66 (SD, 2.47) mL/min per 1.73 m2, the investigators hypothesized that the 2-year eGFR decline in the conservative anemia management group and the aggressive anemia correction group should be 3.32 (SD, 4.94) and 1.03 (SD, 4.94) mL/min per 1.73 m2, respectively. In order to compare the actual efficacy of the intervention with the assumptions above and to evaluate the need for an early termination of the trial, the investigators will perform one interim analysis using a Pocock type α-spending function when a total of 50-60% of the target sample size completed this study or dropped out. Assuming 20% of dropout or lost-to-follow, the planned sample size of 272 patients would yield a power of 90% for group comparison by using t-test with a type I error of 5%.

Regarding cholecalciferol supplementation, 1,000 IU/day would increase serum 25-hydroxyvitamin D level by 11.8 ng/mL in patients with BMI <30, as suggested by the previous trial (Gallagher JC, et al. Ann Intern Med, 2012). The investigators found in our prospective cohort study that the 98.2% of Japanese kidney transplant recipients had BMI <30, and that 10 ng/mL increase in 25-hydroxyvitamin D level was significantly associated with 0.75 mL/min/1.73 m2 less decrease in annual eGFR change independent of potential confounders (in submission). As with the anemia intervention arms above, the investigators will perform one interim analysis using a Pocock type α-spending function when a total of 50-60% of the target sample size completed this study or dropped out in order to compare the actual efficacy of the intervention with the assumptions above and to evaluate the need for an early termination of the trial. Therefore, the investigators expect 1.77 mL/min per 1.73 m2 in eGFR would be preserved by 1,000 IU/day of cholecalciferol supplementation for 2 years. Based on this assumption, this study size will provide a power of 70%.

Estimating kidney function:

In primary analyses, eGFR will be calculated by using the Japanese equation as in sample size calculation (Matsuo S, et al. Am J Kidney Dis, 2009). However, this formula has not yet been validated in kidney transplant recipients. Therefore, the investigators will use the creatinine-based CKD-EPI equation with Japanese coefficient (Stevens LA, et al. Nephrol Dial Transplant, 2010. Horio M, et al. Am J Kidney Dis, 2010) and an available formula if validated in Japanese kidney transplant recipients at the time of analysis.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Factorial
主要目的
Treatment
盲法
None

入排标准

年龄范围
20 Years 至 79 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •≥15 and <60 ml/min per 1.73 m2 of estimated glomerular filtration rate
  • •Transplanted allograft kidney at least 1 year before
  • •<10.5 g/dL of Hb without iron deficiency (serum ferritin level ≥50 ng/ml) or on erythropoiesis stimulating agents treatment regardless of iron status
  • •With written informed consent

排除标准

  • •On anticancer treatment
  • •History of ischemic stroke or transient ischemic attack
  • •Corrected serum calcium ≥10.5 mg/dL
  • •HIV virus infection
  • •Anticipated refractory hypertension by using epoetin beta pegol
  • •In pregnancy and lactation
  • •Current use of native vitamin D supplement
  • •Patients ineligible according to the investigator's judgement

研究组 & 干预措施

Low Hb target without cholecalciferol

No Intervention

Target Hemoglobin level: ≥9.5 and <10.5 g/dL

High Hb target without cholecalciferol

Active Comparator

Target Hemoglobin level: ≥12.5 and <13.5 g/dL

干预措施: High Hb target (Other)

High Hb target with cholecalciferol

Experimental

Target Hemoglobin level: ≥12.5 and <13.5 g/dL Cholecalciferol: 1,000 IU/day

干预措施: High Hb target (Other)

High Hb target with cholecalciferol

Experimental

Target Hemoglobin level: ≥12.5 and <13.5 g/dL Cholecalciferol: 1,000 IU/day

干预措施: cholecalciferol (Dietary Supplement)

Low Hb target with cholecalciferol

Active Comparator

Target Hemoglobin level: ≥9.5 and <10.5 g/dL Cholecalciferol: 1,000 IU/day

干预措施: cholecalciferol (Dietary Supplement)

结局指标

主要结局

Change in allograft kidney function

时间窗: 2 years

As allograft kidney function, GFR is estimated by the modified MDRD equation for Japanese patients with chronic kidney disease.

次要结局

  • Urine markers of kidney injury(6 months)
  • Cardiac biomarkers(2 years)
  • Bone-turnover markers(6 months)
  • Time to the renal composite endpoint(2 years)
  • Time to admission-required cardiovascular events(2 years)
  • Time to all-cause death(2 years)
  • Biopsy-proven acute cellular rejection(2 years)
  • Time to Cancer development or recurrence(2 years)
  • The dose of methoxy polyethylene glycol epoetin beta required to maintain the target hemoglobin level(1 year)
  • Left ventricular mass index(2 years)
  • Blood pressure(2 years)
  • Bone mineral density of lumber spine and femoral neck.(2 years)
  • Hypercalcemia(2 years)

研究者

发起方
CANDLE-KIT Trial Study Group
申办方类型
Other
责任方
Sponsor

研究点 (1)

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