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临床试验/NCT04333745
NCT04333745进行中(未招募)不适用

Influence of Obesity on Oxalate Metabolism and Handling in Calcium Oxalate Stone Formers

University of Alabama at Birmingham2 个研究点 分布在 1 个国家目标入组 22 人开始时间: 2021年9月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
22
试验地点
2
主要终点
Urinary Oxalate Excretion

研究概览

简要总结

The primary goals of this study are to determine the contribution of dietary oxalate absorption, renal oxalate handling, and endogenous oxalate synthesis to urinary oxalate excretion in normal Body Mass Index (BMI) and obese calcium oxalate kidney stone formers.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Basic Science
盲法
None

入排标准

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

入选标准

  • Normal Body Mass Index (≥ 18.5 to < 25); Obese Body Mass Index (≥ 30 to ≤ 45)
  • Able to provide informed consent
  • Willingness to consume controlled diet
  • Composition of most recent stone > 50% calcium oxalate, no uric acid component
  • First time or recurrent calcium oxalate stone former
  • 24-hour urine collections with creatinine values within 20% of appropriate ratio of creatinine (mg)/body weight (kg) for gender, and with creatinine values that are consistent between collections (within 20% of each other)
  • Willingness to stop supplements [vitamins, Ca (citrate or carbonate) and other minerals, herbal supplements, nutritional aids, probiotics] for 14 days before start and during study
  • Willingness to not undertake vigorous exercise during the controlled dietary study
  • Normal fasting blood Comprehensive Metabolic Panel
  • Hemoglobin A1c < 6.5%
  • No food allergies or intolerance to any of the food in study menus
  • Permitted/willing to discontinue medications for kidney stone prevention, including thiazides, allopurinol, and febuxostat and citrate preparations, for 14 days before start and during the studies. They will be instructed to restart these medications at the conclusion of the study

排除标准

  • Abnormal fasting comprehensive metabolic panel (CMP)
  • Hemoglobin A1c (HbA1c) result ≥ 6.5%
  • Estimated Glomerular Filtration Rate (eGFR) <60 ml/min/1.73m^2
  • Primary hyperoxaluria
  • Cystic fibrosis
  • Cystinuria
  • Uric acid stone former
  • Utilization of immunosuppressive medication
  • Nephrotic syndrome
  • Enteric hyperoxaluria
  • Gastrointestinal disorder that could impact oxalate transport
  • Sarcoidosis
  • Uncontrolled hypertension
  • Renal tubular acidosis
  • Primary hyperparathyroidism
  • Liver disease
  • Neurogenic bladder
  • Urinary diversion
  • Chronic diarrhea
  • Bariatric surgery
  • Active malignancy or treatment for malignancy within 12 months prior to screening
  • Pregnancy
  • Breast feeding/nursing
  • Females of child bearing age who are not able to use an effective method of birth control during the study
  • Mental/medical condition that is likely to impede successful study completion
  • Illness including flu / common cold / fever 14 days before study and during study
  • Diarrhea or other abnormal gastrointestinal event (e.g. abnormal bowel movements) 14 days before study or during study
  • Antibiotic use within last 6 months (based on recommendations of the NIH Human Microbiome Project, Protocol A)
  • Inability or unwillingness to undergo MRI

研究组 & 干预措施

Controlled Dietary Study

Experimental

Participants will consume the controlled diet for five days. After one day on the diet, subjects will provide three 24-hour urine collections. On the last dayof the diet, subjects will come in a fasted state to ingest a small amount of carbon-13 oxalate and sucralose, with hourly urine collections and blood samples being taken before and after the ingestion.

干预措施: Controlled Diet (Other)

Controlled Dietary Study

Experimental

Participants will consume the controlled diet for five days. After one day on the diet, subjects will provide three 24-hour urine collections. On the last dayof the diet, subjects will come in a fasted state to ingest a small amount of carbon-13 oxalate and sucralose, with hourly urine collections and blood samples being taken before and after the ingestion.

干预措施: Carbon-13 Oxalate and Sucralose Ingestion (Dietary Supplement)

结局指标

主要结局

Urinary Oxalate Excretion

时间窗: Baseline through Day 5

Urinary oxalate excretion from urine samples will be measured as mg/day

次要结局

未报告次要终点

研究者

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

Dean Assimos, MD

Principal Investigator

University of Alabama at Birmingham

研究点 (2)

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