NYC Heart Follow-Up Study 2010

Sodium Clinical Trial

— HFUS  

Official title:

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

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01889589
• Other study ID #: NYCHFUS2010
• Status: Completed
• Phase: N/A
• First received: June 26, 2013
• Last updated: June 27, 2013
• Start date: April 2010
• Est. completion date: September 2010

Study information

• Verified date: June 2013
• Source: New York City Department of Health and Mental Hygiene
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Institutional Review Board
• Study type: Observational

Clinical Trial Summary

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

Recruitment information / eligibility

• Status: Completed
• Enrollment: 1775
• Est. completion date: September 2010
• Est. primary completion date: September 2010
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Both
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• > 18 Years

Exclusion Criteria:

• Pregnant, breastfeeding or lactating; past or current dialysis

Study Design

Time Perspective: Cross-Sectional

Related Conditions & MeSH terms

• Sodium

Intervention

Other:
• Surveillance

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
New York City Department of Health and Mental Hygiene

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	24-hour urinary sodium		24-hour period	No