Effects of Barley Green in Patients With Hyperuricemia

  • STATUS
    Recruiting
  • participants needed
    130
  • sponsor
    Second Affiliated Hospital, School of Medicine, Zhejiang University
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Updated on 19 February 2024
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Summary

This experiment evaluates the effect of Barley Green in patients with hyperuricemia and explores the effect of Barley Green on metabolic indexes such as uric acid, blood lipids, blood glucose, free fatty acids130 adult participants , age 18 to 65 years, will be randomized into one of the two arms. Arm A (control group) will receive dietary guidance. Arm B will receive dietary guidance and Barley Green.

Details
Condition Dietary Supplement
Age 18years - 65years
Treatment Group A, Group B
Clinical Study IdentifierNCT04438486
SponsorSecond Affiliated Hospital, School of Medicine, Zhejiang University
Last Modified on19 February 2024

Eligibility

 Yes No Not Sure

Inclusion Criteria

Age 18-65 years old those who are willing to accept assessment and sign
informed consent
Under the normal purine diet, two fasting blood uric acid levels on different
days: 420umol/l <blood uric acid <540 umol/l (male), 360 umol/l <blood uric
acid <540 umol/l (female)

Exclusion Criteria

Patients currently receiving treatment for hyperuricemia Suffering from
diseases that affect the digestion and absorption(such as chronic diarrhea
constipation, severe gastrointestinal inflammation, active gastrointestinal
ulcers, after gastrointestinal resection, cholecystitis/cholecystectomy, etc.)
Suffering from cardiovascular and cerebrovascular diseases, grade 3
hypertension, chronic hepatitis, malignant tumors, anemia, mental illness and
memory disorders, epilepsy and other diseases; At the same time receive other
functional food nutrition support (plant active substances, health food)
Patients with abnormal liver function (alanine aminotransferase or/and
aspartate aminotransferase exceeds 3 times the upper limit of normal value)
patients with abnormal renal function (serum creatinine exceeds the upper
limit of normal value) Suffering from infectious diseases such as active
tuberculosis and AIDS; People who are severely allergic to the ingredients of
research During pregnancy or lactation; Patients with physical disabilities
and clinicians think it is not suitable to participate in the study (for
example, suffering from serious diseases not included in the discharge
criteria) Gouty arthritis attack 2 times; One episode of gouty arthritis with
blood uric acid >480 umol/l, or any of the following: age <40 years old
evidence of gout stone or urate deposition in the joint cavity, uric acid
nephrolithiasis or renal impairment (GFR89ml/(min1.73m2)), hypertension
impaired glucose tolerance or diabetes, dyslipidemia, obesity, coronary heart
disease, stroke, cardiac insufficiency; Blood uric acid>480 umol/l combined
with any of the following: uric acid nephrolithiasis or renal impairment
(GFR89ml/(min1.73m2)), hypertension, impaired glucose tolerance or diabetes
dyslipidemia, obesity, Coronary heart disease, stroke, heart failure
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