Pre-ESRD Syndrome in High Risk African Americans

Evaluation of the dipping status of blood pressure (wether blood pressure decreases at night) and renal functional reserve and wether non-dippers (those whose blood pressure does not decrease at night) can be modulated to dippers with potassium treatment...

Date First Received: September 21, 2005

Last Updated: December 7, 2007

Verified by: National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK), December 2007

Clinical Trial Phase: N/A | Start Date: July 2002

Overall Status: Terminated

Estimated Enrollment: 144

Brief Summary

Official Title: “Pre-ESRD Syndrome in High Risk African American Young Adults”

Condition Keyword(s):

Intervention(s):

Evaluation of the dipping status of blood pressure (wether blood pressure decreases at night) and renal functional reserve and wether non-dippers (those whose blood pressure does not decrease at night) can be modulated to dippers with potassium treatment.

Study Type: Interventional

Study Design: Prevention, Randomized, Double-Blind, Placebo Control, Parallel Assignment

Detailed Clinical Trial Description

Evaluation of the dipping status of blood pressure (wether blood pressure decreases at night) and renal functional reserve and wether non-dippers (those whose blood pressure does not decrease at night) can be modulated to dippers with potassium treatment.

Intervention(s) in this Clinical Trial

  • Drug: Potassium Chloride

Criteria for Participation in this Clinical Trial

  • Inclusion Criteria: 18-35, healthy volunteers, African American
  • Exclusion Criteria: Active medical conditions, prescription drug therapy other than birth control

Gender Eligibility for this Clinical Trial: Both

Minimum Age for this Clinical Trial: 18 Years

Maximum Age for this Clinical Trial: 35 Years

Are Healthy Volunteers Accepted for this Clinical Trial?: Accepts Healthy Volunteers

Clinical Trial Sponsor Information

Lead Sponsor: National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

Overall Clinical Trial Officials and Contacts

Elizabeth B Ripley, MD Principal Investigator Virginia Commonwealth University  

Additional Information

Information obtained from ClinicalTrials.gov on August 29, 2008

Link to the current ClinicalTrials.gov record. http://clinicaltrials.gov/show/NCT00224939

Study ID Number: DK 62714

ClinicalTrials.gov Identifier: NCT00224939

Health Authority: United States: Federal Government

Clinical Trials Authorship and Review

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