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临床试验/NCT03301558
NCT03301558
撤回
2 期

The Effect of Sodium Bicarbonate (Nephrotrans®) on Calcification Propensity of Serum in Kidney Transplant Recipients

Prim. Priv. Doz. Dr. Daniel Cejka2 个研究点 分布在 1 个国家2025年12月31日

概览

阶段
2 期
干预措施
Low dose sodium bicarbonate
疾病 / 适应症
Kidney Transplant; Complications
发起方
Prim. Priv. Doz. Dr. Daniel Cejka
试验地点
2
主要终点
Propensity of serum for calcification
状态
撤回
最后更新
5天前

概览

简要总结

This is a single-center, prospective, open-label, randomized, cross-over study.

详细描述

The primary hypothesis (H1) is that the T50 value will change between wash-out and high-dose (3000mg/d) sodium bicarbonate (Nephrotrans®) substitution. The 0-hypothesis (H0) is that substitution of 3000 mg/d sodium bicarbonate (Nephrotrans®) has no effect on T50-values as compared to wash-out-phase. Patients will be randomized in a 1:1 ratio to either receive low-dose (1500 mg/d) sodium bicarbonate followed by high-dose (3000mg/d) sodium bicarbonate (sequence A-B) or to receive high-dose sodium bicarbonate followed by low-dose sodium bicarbonate (sequence B-A) with washout-phases in between. Patients will be randomized in a 1:1 ratio to either receive low-dose (1500 mg/d) sodium bicarbonate followed by high-dose (3000mg/d) sodium bicarbonate (sequence A-B) or to receive high-dose sodium bicarbonate followed by low-dose sodium bicarbonate (sequence B-A) with washout-phases in between. The study will start with an initial run-in wash-out phase, where all sodium bicarbonate or other alkalizing treatment taken by the patient as standard of care will be discontinued. Consequently, there will be a sodium bicarbonate treatment (high dose/low dose) phase, followed by a wash-out phase, followed by another sodium bicarbonate treatment (high dose/low dose) phase, followed by a final wash-out phase. Each study phase, including wash-out phases as well as low-dose and high-dose treatment phases will be 14 ±3 days of duration. Patients will be followed up to 12weeks after randomization until the last study visit of the final wash-out phase.

注册库
clinicaltrials.gov
开始日期
2025年12月31日
结束日期
2025年12月31日
最后更新
5天前
研究类型
Interventional
研究设计
Crossover
性别
All

研究者

发起方
Prim. Priv. Doz. Dr. Daniel Cejka
责任方
Sponsor Investigator
主要研究者

Prim. Priv. Doz. Dr. Daniel Cejka

Head of Nephrology

Elisabethinen Hospital

入排标准

入选标准

  • Adults ≥ 18 years old
  • Prevalent (≥ 6 months after kidney transplantation) kidney transplant recipients
  • eGFR (CKD-EPI formula) between 10 and 50 ml/min/1.73 m²
  • Patient has provided informed consent prior to initiation of any study related procedure

排除标准

  • Allergy to sodium bicarbonate or any component of Nephrotrans®, namely soy or peanuts (reported cross-reactivity to peanuts has been reported in patients with soy-allergy).
  • Unstable clinical condition (e.g. uncontrolled heart failure, clinical uremia, uncontrolled hypertension, impending initiation of dialysis treatment…) as judged by the recruiting physician
  • Pregnant and nursing (lactating) women
  • Unwillingness to discontinue current medication with sodium bicarbonate
  • Unwillingness to discontinue antacids containing aluminum, calcium carbonate, magnesium, lactate, citrate, bicarbonate or mixtures thereof

研究组 & 干预措施

Low dose sodium bicarbonate

Low dose 1500 mg sodium bicarbonate (Nephrotrans®) per day (500mg tablets 3x/day) for 14 ± 3 days. The patients will be advised to take one capsule with breakfast, one with lunch and one with dinner (schedule 1-1-1).

干预措施: Low dose sodium bicarbonate

High Dose sodium bicarbonate

High dose 3000 mg of sodium bicarbonate (Nephrotrans®) per day (500mg tablets 3x/day) for 14 ± 3 days. The patients will be advised to take two capsules with breakfast, two with lunch and two with dinner (schedule 2-2-2).

干预措施: High dose sodium bicarbonate

结局指标

主要结局

Propensity of serum for calcification

时间窗: 12 weeks

The primary outcome is change in the mean T50 values between different study phases (treatment vs. control).

次要结局

  • Serum bicarbonate levels(12 weeks)

研究点 (2)

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