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临床试验/NCT05460247
NCT05460247招募中不适用

The Effect of Protein Sources on Urinary Stone Risk

Washington University School of Medicine2 个研究点 分布在 1 个国家目标入组 14 人开始时间: 2022年10月30日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
14
试验地点
2
主要终点
Urinary stone risk

研究概览

简要总结

Prior studies have shown that the source of dietary protein can have a significant impact on urinary stone risk. However, whey and plant protein isolates have not been compared. This is an important distinction as protein supplements fortified foods are increasingly popular. Herein, we seek to investigate the effect of different protein supplements, in an otherwise identical diet, on urinary stone risk.

详细描述

Each participant will receive a pre-made diet for 5 days at a time, for a total of 4 cycles. Previous studies have shown urine values reach a constant within the first 3 days. Diet will be a constant baseline diet representative of a standard Mediterranean diet. Participants will receive this diet to eat at home for 5 days with a supplemental protein shake at each meal (3 times a day). Participants will be required to drink 2.5-3 liters of fluid daily. Caffeine may be ingested as caffeine pills. Excessive exercise will be discouraged during the treatment phase.

Diet will remain constant with respect to protein quantity and all other ingredients and will only change protein isolate source in supplemental protein shake.

On days 4 and 5 of the diet, participants will be asked to collect two consecutive 24-hour urines. Between each 5-day diet phase, a flexible washout period will be allowed in which participants may eat a self-selected diet to take a break from standardized meals. Participants may resume the next phase diet on a day which is convenient for planned 24-hour urine collection at the end of that phase. The break period is to last no longer than 10 days.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Crossover
主要目的
Treatment
盲法
Single (Participant)

入排标准

年龄范围
18 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Willing and able to complete the study
  • Healthy with no personal or family history of kidney stones

排除标准

  • Allergy to any protein isolates or menu items used in the study
  • History of calcium oxalate, cysteine, uric acid, or infection stones
  • Disorders of absorption: Celiac disease, Irritable Bowel Disease, chronic diarrhea, short gut
  • Systemic predisposition to stones: gout, congenital hyperuricemia, chronic diarrhea, insulin resistance, neoplastic disorders, hyperparathyroidism or renal tubular acidosis
  • Women who are currently pregnant or planning pregnancy within 2 years
  • Renal transplant recipient
  • Bedridden study participants (ECOG ≥ 3)
  • Uncorrected anatomical obstruction of the urinary tract
  • History of recurrent urinary tract infections (> 3 urinary tract infections/year proven by urine culture)
  • Exclusions due to medication use:
  • Chronic use of lithium
  • Long-term glucocorticoid use (> 7.5 mg prednisone daily for > 30 days prior to enrollment)
  • Intake of narcotic medication on a daily basis for >30 days prior to enrollment
  • Supplemental Vitamin C (> 1 g daily)
  • Carbonic anhydrase inhibitors (acetazolamide, topiramate, zonisamide)
  • high dose calcium supplementation (> 1,200 mg daily)
  • Medications that may crystallize in the urine (guaifenesin, sulfonamides, triamterene, and the protease inhibitors indinavir and nelfinavir).
  • Non-English Speakers
  • History of Syndrome of Inappropriate Antidiuretic Hormone Secretion (SIADH)
  • Anatomical urologic abnormalities including ileal conduits, horseshoe kidney, megaureter or solitary kidney
  • Psychiatric conditions impairing compliance with the study
  • Vulnerable population (prisoner and/or cognitive impairment that the investigator feels will impact participant's ability to complete study activities)

结局指标

主要结局

Urinary stone risk

时间窗: 3 months after beginning study

24 hour urine panel and supersaturation for Calcium Oxalate and Uric Acid

Calcium Oxalate Inhibitor activity

时间窗: 3-6 months after beginning study

mmol of Oxalate added before spontaneous precipitation

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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