Chronic Hepatitis C Clinical Trial
| 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 |
| 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 |
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.
| 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 |
N/A
| Country | Name | City | State |
|---|---|---|---|
| Israel | Hillel Yaffe Medical Center | Hadera |
| Lead Sponsor | Collaborator |
|---|---|
| Hillel Yaffe Medical Center |
Israel,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | To increase the sustained virological response | One year | No |
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