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临床试验/NL-OMON49499
NL-OMON49499已完成不适用

Butyrate: effect of oral administration in patients with mild hypertension - BEAM study

Academisch Medisch Centrum0 个研究点目标入组 50 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
50

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 至 99(—)

入选标准

  • - Age between 40 and 65 years
  • - For females: postmenopausal status
  • - Caucasian
  • - Mild hypertension (defined as systolic blood pressure range 140-159 mmHg
  • and/or diastolic blood pressure range 90-100 mmHg) without antihypertensive
  • medication OR use of 1 antihypertensive drug due to hypertension and willing to
  • temporarily stop this medication
  • - Body mass index (BMI) lower than 27 kg/m2

排除标准

  • - Insufficient knowledge of the Dutch language
  • - Use of betablockers
  • - Known secondary causes of hypertension such as renal artery stenosis, adrenal
  • or thyroid disease
  • - History of cardiovascular disease: angina pectoris, myocardial infarction,
  • cerebrovascular accident, transient ischemic attack, peripheral artery disease,
  • heart failure.
  • - History of diabetes mellitus
  • - Current smoking
  • - Antibiotics usage within three months before inclusion
  • - Having a severe disease of the digestive tract, such as celiac disease,
  • Crohn*s disease, active ulcerative colitis or short bowel syndrome.
  • - Impaired renal function, defined as an estimated glomerular filtration rate
  • (eGFR) lower than 60 ml/min/1,73m2 using the CKD-EPI formula within a period of
  • two years before the screening visit. Participants without an available lab
  • result on renal function will not be included.

研究者

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