- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00172302
Can Intravenous Vitamin C Improve Skin Hyperpigmentation in Long-Term Hemodialysis Patients?
September 12, 2005 updated by: National Taiwan University Hospital
Intravenous vitamin C may improve skin hyperpigmentation in chronic hemodialysis patients
Study Overview
Status
Unknown
Conditions
Intervention / Treatment
Detailed Description
Melanogenesis is caused by enzymatic conversion of tyrosine to melanin pigments.Ascorbic acid has the ability to inhibit peroxidase and may thus inhibit melanin synthesis.
Study Type
Interventional
Enrollment
40
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
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Taipei, Taiwan, 100
- National Taiwan University Hospital
-
Contact:
- Tze-Wah Kao, MD
- Phone Number: 886-2-2356-2000
- Email: twkao@ha.mc.ntu.edu.tw
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Principal Investigator:
- Tze-Wah Kao, MD
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
20 years to 80 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- chronic hemodialysis patients
Exclusion Criteria:
- allergic to vitamin C, using steroid, etc
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: Double
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
---|
Skin pigmentation extent
|
Secondary Outcome Measures
Outcome Measure |
---|
blood anti-oxidant level
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Kao Tze-Wah, MD, National Taiwan University Hospital
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
November 1, 2005
Study Registration Dates
First Submitted
September 12, 2005
First Submitted That Met QC Criteria
September 12, 2005
First Posted (Estimate)
September 15, 2005
Study Record Updates
Last Update Posted (Estimate)
September 15, 2005
Last Update Submitted That Met QC Criteria
September 12, 2005
Last Verified
May 1, 2005
More Information
Terms related to this study
Additional Relevant MeSH Terms
- Skin Diseases
- Kidney Diseases
- Urologic Diseases
- Renal Insufficiency, Chronic
- Pigmentation Disorders
- Kidney Failure, Chronic
- Renal Insufficiency
- Hyperpigmentation
- Physiological Effects of Drugs
- Molecular Mechanisms of Pharmacological Action
- Protective Agents
- Micronutrients
- Vitamins
- Antioxidants
- Ascorbic Acid
Other Study ID Numbers
- 930105
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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