NCT03154502

Brief 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.

Trial Health

100
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
130

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Mar 2015

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

March 1, 2015

Completed
1.7 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 30, 2016

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

October 30, 2016

Completed
6 months until next milestone

First Submitted

Initial submission to the registry

May 12, 2017

Completed
4 days until next milestone

First Posted

Study publicly available on registry

May 16, 2017

Completed
Last Updated

May 16, 2017

Status Verified

May 1, 2017

Enrollment Period

1.7 years

First QC Date

May 12, 2017

Last Update Submit

May 12, 2017

Conditions

Dietary HabitsRisk Factor, CardiovascularNutritional Disorder

Keywords

Sodium intakeUrinary sodium excretion

Outcome Measures

Primary Outcomes (1)

  • Urinary sodium excretion

    Amount of sodium in 24h urine collection

    1 year

Interventions

Urinary sodium excretionDIAGNOSTIC_TEST

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

Eligibility Criteria

Age25 Years - 64 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)
Sampling MethodProbability Sample
Study Population

Will be enrolled a sample of 178 adults aged 25 to 64 years. The research team, who have faculty appointments in USFQ, supervised the collection of the urine samples. We invited a broad spectrum of employees (which included health care workers, professors, and custodial staff) from both institutions to participate in the study.

You may qualify if:

  • None

You may not qualify if:

  • 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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Biospecimen

Retention: SAMPLES WITHOUT DNA

Urine

MeSH Terms

Conditions

Feeding BehaviorNutrition Disorders

Condition Hierarchy (Ancestors)

Behavior, AnimalBehaviorNutritional and Metabolic Diseases

Study Officials

  • Enrique Teran, MD, PhD

    Universidad San Francisco de Quito

    STUDY DIRECTOR

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
CROSS SECTIONAL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Associate Professor

Study Record Dates

First Submitted

May 12, 2017

First Posted

May 16, 2017

Study Start

March 1, 2015

Primary Completion

October 30, 2016

Study Completion

October 30, 2016

Last Updated

May 16, 2017

Record last verified: 2017-05

Data Sharing

IPD Sharing
Will not share