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NCT00804752 Clinical Trial

Vitamin D Treatment in Patients With Chronic Hepatitis C

Chronic Hepatitis C Clinical Trial

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT00804752
Other study ID # 0040-08-HYMC
Secondary ID
Status Recruiting
Phase N/A
First received December 7, 2008
Last updated December 8, 2008

Study information
Verified date December 2008
Source Hillel Yaffe Medical Center
Contact n/a
Is FDA regulated No
Health authority Israel: Ministry of Health
Study type Interventional

Clinical Trial Summary

We hypothesize that patients with Ch.HCV have a low level of vitamin D, and that by raising their vitamin D levels by adding it to their standard treament of Pegylated Interferon and Ribavirin, there will be an increase in their sustained virological response.

Recruitment information / eligibility
Status Recruiting
Enrollment 0
Est. completion date
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Chronic Hepatitis C Genotype 1

Exclusion Criteria:

- Vitamin D intoxication Renal Failure Liver Failure Malignancy

Study Design

N/A

Related Conditions & MeSH terms

Intervention

Drug:
• Adding vitamin D
Adding 1000IU/Vitamin D daily
• Vitamin D
Addition of 1000IU/day Vitamin D

Locations
Country Name City State
Israel Hillel Yaffe Medical Center Hadera

Sponsors (1)
Lead Sponsor Collaborator
Hillel Yaffe Medical Center

Country where clinical trial is conducted

Israel, 

Outcome
Type Measure Description Time frame Safety issue
Primary To increase the sustained virological response One year No
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