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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04041115
Other study ID # MICTLAN-2
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 2016
Est. completion date August 15, 2022

Study information

Verified date March 2019
Source Instituto Nacional de Ciencias Medicas y Nutricion Salvador Zubiran
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The implementation of nutritional strategies targeting several variables at once could benefit patients with cirrhosis. Non-alcoholic beer has different compounds derived from hops that exert antioxidant, anti-inflammatory and nutritional properties. The aim of this study is to evaluate the effect of diet + exercise and non-alcoholic beer on nutritional status, endothelial function and quality of life in patients with cirrhosis.


Recruitment information / eligibility

Status Completed
Enrollment 42
Est. completion date August 15, 2022
Est. primary completion date December 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria: - Liver Cirrhosis of any aetiology (liver biopsy or a combination of clinical and biochemical variables plus evidence of portal hypertension); without decompensation during the past month; serum creatinine <1.5 mg%; able to attend the appointed visits and willing to participate in the study. Exclusion Criteria: - Severe concomitant cardiopulmonary diseases; decompensated type 2 Diabetes Mellitus, insulin use or proliferative diabetic retinopathy; orthopedic or osteomuscular limitations; any type of cancer; primary sclerosing cholangitis and inflammatory bowel disease.

Study Design


Intervention

Dietary Supplement:
Non-alcoholic beer
Treatment consisted of 330ml non-alcoholic beer per day, plus an individualized dietary program and an exercise program with a pedometer-based bracelet to reach at least 5000 steps/day during 2 + 8 weeks.
Other:
control
Treatment consisted of 330ml of water, plus an individualized dietary program and an exercise program with a pedometer-based bracelet to reach at least 5000 steps/day during 2 + 8 weeks.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Instituto Nacional de Ciencias Medicas y Nutricion Salvador Zubiran

Outcome

Type Measure Description Time frame Safety issue
Primary Nutritional status improvement in impedance-derived phase angle (PhA) 8 weeks
Primary Endothelial function improvement in flow-mediated dilation (brachial artery) 8 weeks
Primary Endothelial dysfunction improvement in serum markers of endothelial function (v.gr. nitric oxide, NO; prostacyclin, PGI2, etc.) 8 weeks
Primary Quality of life questionnaire Improvement in quality of life questionnaire CLDQ (chronic liver disease questionnaire) 8 weeks
Primary Changes in the heterogeneity of gut Microbiota Changes in the heterogeneity of fecal microbiota in terms of bacterial diversity will be assessed 8 weeks
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