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NCT03154502 Clinical Trial

Sodium Intake in Ecuadorian Population

Dietary Habits Clinical Trial

Official title:
Sodium Urinary Excretion Measurement in Ecuadorian Population

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT03154502
Other study ID # HUBI-1022
Secondary ID
Status Completed
Phase N/A
First received May 12, 2017
Last updated May 12, 2017
Start date March 1, 2015
Est. completion date October 30, 2016

Study information
Verified date May 2017
Source Universidad San Francisco de Quito
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This study is aim to determine the sodium intake in Ecuadorian population that is an unknown information at present. For that, 24h urine samples will be collected from 130 subjects working either at tue USFQ or HDLV to measure sodium excretion.

Recruitment information / eligibility
Status Completed
Enrollment 130
Est. completion date October 30, 2016
Est. primary completion date October 30, 2016
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 25 Years to 64 Years
Eligibility Inclusion Criteria:

Exclusion Criteria:

- unable to provide informed consent

- unable to provide 24-hr urine excretion sample

- those with a known history of heart or kidney failure, stroke, and liver disease

- those using diuretics, multivitamins, NSADs, or prostaglandins during the last two weeks

- pregnant women

Study Design

Related Conditions & MeSH terms

Intervention

Diagnostic Test:
• Urinary sodium excretion
Urinary sodium and potassium were measured using the Ion-Selective Electrode (ISE) indirect Na-K-Cl for Gen.2 (Roche Diagnostic, Switzerland).

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
Universidad San Francisco de Quito

Outcome
Type Measure Description Time frame Safety issue
Primary Urinary sodium excretion Amount of sodium in 24h urine collection 1 year
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