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Clinical Trials/RPCEC00000268
RPCEC00000268
Completed
N/A

Pilot study to identify candidates for biomarkers associated with Cape gooseberry consumption

CORPOICA0 sites20 target enrollmentApril 17, 2018

Overview

Phase
N/A
Intervention
Not specified
Conditions
ot applicable. The study seeks to identify biomarkers associated with the acute and chronic consumption of cape gooseberry, and the impact of this consumption on the composition of the intestinal microbiota.
Sponsor
CORPOICA
Enrollment
20
Status
Completed
Last Updated
last year

Overview

Brief Summary

See attachment

Registry
who.int
Start Date
April 17, 2018
End Date
March 3, 2020
Last Updated
last year
Study Type
Interventional
Sex
Male

Investigators

Sponsor
CORPOICA

Eligibility Criteria

Inclusion Criteria

  • 1\.Male volunteers
  • 2\.With age \=20 and \=50 y
  • 3\.BMI between 18\.8 Kg / mt2 and 24\.9 Kg / mt2,
  • 4\.Consumers of cape gooseberries and citrus fruits
  • 5\.Non\-smokers
  • 6\.Non\- high performance athlete (subjects with a sedentary physical activity, mild or moderate, without exceeding 10 hours per week of training).
  • 7\.No history and/or diagnosis of chronic diseases (cardiovascular, hypertension, congestive heart failure, stroke, arrhythmias, dyslipidemia, diabetes mellitus, cancer, chronic renal failure, liver disorders, hypothyroidism, insomnia, duodenal ulcer, gastritis, disorders of malignancy absorption, Alzheimer's, Parkinson's or any other neurodegenerative disease that prevents an adequate collection of information, cancer, Crohn's disease, ulcerative colitis, short bowel syndrome or celiac disease, dysautonomies, sleep disorders and psychiatric disorders)
  • 8\.Not currently consuming medication (lipid\-lowering drugs, antioxidant supplements, natural products, supplements or dietary supplements, multivitamins, antiepileptics, steroidal anti\-inflammatories, hypnotic drugs)
  • 9\.Without antibiotic or antiparasitic use in the last three months.
  • 10\.Volunteers should have a work schedule between 7\.00 a.m. and 6\.00 p.m. from Monday to Friday and not having to leave the workplace during the time the study lasts.

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Not specified

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