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OpenTrials
Completed

NCT Number: NCT01889589

NYC Heart Follow-Up Study 2010

This surveillance project will assess NYC population sodium intake using the gold standard measurement of 24-hour urine collection. This surveillance project is a critical component of a larger initiative, coordinated by NYC, to reduce sodium intake nationwide through voluntary industry reductions in processed food sodium content. The project will assess current population sodium intake, against which population intake changes at three years can be assessed

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Key information

Conditions

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

New York, United States

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • > 18 Years

Exclusion criteria

  • Pregnant, breastfeeding or lactating; past or current dialysis

Treatment and study plan

Surveillance

Other

Primary outcomes

  1. 24-hour urinary sodium

    Time frame: 24-hour period

Sponsors and collaborators

Lead sponsor

New York City Department of Health and Mental Hygiene

Other Gov

Registry information

Official study title

Baseline 24 Hour Urine Collection in Population-based Sample of NYC Adults

Acronym: HFUS

Important dates

Study start
2010
Primary completion
2010
Study completion
2010
First posted
Jun 28, 2013
Registry last updated
Jun 28, 2013

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.