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NCT01454193 Clinical Trial

Are we Loading Our Patients With Sodium During Hemodialysis Treatments?

Renal Failure Clinical Trial

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT01454193
Other study ID # 078-08
Secondary ID
Status Completed
Phase N/A
First received October 13, 2011
Last updated October 18, 2011
Start date January 2001
Est. completion date October 2011

Study information
Verified date October 2011
Source Renal Research Institute
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Observational

Clinical Trial Summary

The objectives of the data search is to find out if there is correlation between pre, post serum sodium concentration, dialysate sodium concentration, interdialytic weight gain and associated changes in pre and post systolic and diastolic blood pressure, mean arterial pressure, number of blood pressure medications and adherence to 3 times per week dialysis, mortality.

Recruitment information / eligibility
Status Completed
Enrollment 10000
Est. completion date October 2011
Est. primary completion date October 2011
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 88 Years
Eligibility Inclusion Criteria:

- Hemodialysis patient

Study Design

Observational Model: Cohort, Time Perspective: Retrospective

Related Conditions & MeSH terms

Locations
Country Name City State
United States Renal Research Institute New York New York

Sponsors (1)
Lead Sponsor Collaborator
Renal Research Institute

Country where clinical trial is conducted

United States, 

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