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Clinical Trial Details — Status: Unknown status

Administrative data

NCT number NCT00396396
Other study ID # EVMS 06-03-FB-0044
Secondary ID
Status Unknown status
Phase N/A
First received November 3, 2006
Last updated November 3, 2006
Start date October 2006

Study information

Verified date November 2006
Source Eastern Virginia Medical School
Contact Ritche Chiu, MD
Phone 757-680-0211
Email dr_ritchechiu@yahoo.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to investigate the exact role of Acetylcysteine (Mucomyst) in altering creatinine clearance. Prior studies have shown the protective effects of Acetylcysteine on contrast-induced renal dysfunction. In these studies, Acetylcysteine lowered the incidence of serum creatinine elevation after administration of radiographic contrast agents. Not only was the increase in serum creatinine prevented, the studies also demonstrated a significant increase in creatinine clearance after administration of the agent. These prior studies did not evaluate if the increase in creatinine clearance was indeed from a protective benefit of Acetylcysteine in preserving the GFR versus simply increasing the proximal tubular creatinine secretion without actually affecting the GFR. We propose an experiment to help support our hypothesis that Acetylcysteine increases creatinine clearance via an increase in proximal tubular secretion of creatinine.


Recruitment information / eligibility

Status Unknown status
Enrollment 35
Est. completion date
Est. primary completion date
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 79 Years
Eligibility Inclusion Criteria:

1. Between the ages of 18 and 79 years

2. In good general health

3. Able to provide informed consent

Exclusion Criteria:

1. Allergy to acetylcysteine or cimetidine,

2. Age less than 18 years or greater than 79 years of age,

3. Women of childbearing age and not able to use adequate contraception, or 4. Anyone currently on any medication that interferes with tubular secretion of creatinine such as trimethoprim-sulfamethoxazole (Bactrim).

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Acetylcysteine


Locations

Country Name City State
United States Eastern Virginia Medical School/Nephrology Associates Norfolk Virginia

Sponsors (1)

Lead Sponsor Collaborator
Eastern Virginia Medical School

Country where clinical trial is conducted

United States, 

See also
  Status Clinical Trial Phase
Completed NCT04375358 - Creatinine Clearance as a Predictor of Successful Withdrawl of Continuous Renal Replacement Therapy in Intensive Care