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临床试验/NCT05365477
NCT05365477已完成4 期

Randomized Trial of Empiric Versus Selective Prevention Strategies for Kidney Stone Disease

Vanderbilt University Medical Center2 个研究点 分布在 1 个国家目标入组 56 人开始时间: 2022年8月4日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
已完成
入组人数
56
试验地点
2
主要终点
Calcium oxalate supersaturation

研究概览

简要总结

The aims of this study are to 1) Conduct a randomized clinical trial of selective versus empiric diet plus pharmacologic therapy in high-risk stone formers and 2) Determine adverse effects from, and adherence to selective and empiric strategies.

详细描述

Diet and pharmacologic interventions for preventing future kidney stone episodes are effective, however clinical guideline panels disagree on whether clinicians should perform selective therapy: performing 24-hour urine testing to guide choosing interventions to correct abnormal urinary parameters. The alternative strategy is empiric therapy: applying interventions without 24-hour urine testing. While 24-hour urine testing is considered the standard of care by nephrology and urology specialties for higher risk patients, the American College of Physicians does not recommend 24-hour urine testing.

This is a randomized clinical trial of selective versus empiric therapy for patients with presumed idiopathic calcium stone disease, representing >80% of the kidney stone population. The primary outcome is change in urinary supersaturation, which associates with symptomatic stone recurrence. We will recruit patients with presumed idiopathic calcium stone disease with at least 2 stone events within the previous 5 years. Participants will be randomly assigned to empiric diet plus thiazide with potassium citrate daily, or to selective diet plus pharmacologic therapy based on the 24-hour urine abnormalities identified at baseline and adjusted during follow-up. The primary outcomes will be the calculated calcium oxalate and calcium phosphate supersaturations. In addition, we will determine adverse effects from, and adherence to, selective and empiric strategies.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Two or more symptomatic kidney stone events in the last 5 years

排除标准

  • Medullary sponge kidney or renal tubular acidosis
  • Untreated urinary obstruction
  • Primary hyperparathyroidism
  • Primary hyperoxaluria
  • Pregnancy
  • Inflammatory bowel disease or bowel resection
  • Sarcoidosis
  • Cystinuria
  • Prior stone composition with uric acid, struvite, cystine, carbonate apatite
  • Use of specific medications (thiazides, topiramate, xanthine oxidase inhibitors, citrate, bicarbonate)
  • Chronic kidney disease stage 3 or higher (eGFR<60)
  • Gouty arthritis or 3 gout episodes in 1 year
  • Known allergy to study medications
  • Hypokalemia or hyponatremia at screening.
  • Age < 18 years

研究组 & 干预措施

Empiric Therapy

Active Comparator

Diet intervention and drug intervention not based on 24 hour urine results

干预措施: Empiric Therapy: Diet (Behavioral)

Empiric Therapy

Active Comparator

Diet intervention and drug intervention not based on 24 hour urine results

干预措施: Empiric Therapy: Drug (Drug)

Selective Therapy

Experimental

Diet intervention and drug intervention based on 24 hour urine results

干预措施: Selective Therapy: Diet (Behavioral)

Selective Therapy

Experimental

Diet intervention and drug intervention based on 24 hour urine results

干预措施: Selective Therapy: Drug (Drug)

结局指标

主要结局

Calcium oxalate supersaturation

时间窗: Baseline compared to two months

Calculated calcium oxalate supersaturation in urine

Calcium phosphate supersaturation

时间窗: Baseline compared to two months

Calculated calcium phosphate supersaturation in urine

次要结局

  • Uric acid supersaturation(Baseline compared to two months)
  • 24hr urine parameters(Baseline compared to two months)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

David Penson

Professor and Chair, Department of Urology

Vanderbilt University Medical Center

研究点 (2)

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