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EFFECT OF VITAMIN D REPLACEMENT ASSOCIATED WITH ADAPTIVE IMMUNE RESPONSE IN CHRONIC HEPATITIS C PATIENTS WITH VITAMIN D DEFICIENCY

EFFECT OF VITAMIN D REPLACEMENT ASSOCIATED WITH ADAPTIVE IMMUNE RESPONSE IN CHRONIC HEPATITIS C PATIENTS WITH VITAMIN D DEFICIENCY

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
TCTR
Registry ID
TCTR20160429001
Enrollment
Unknown
Registered
2016-04-29
Start date
2014-01-01
Completion date
Unknown
Last updated
2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Vitamin D deficiency Chronic Hepatitis C T&#45

Interventions

The dosages of ergocalciferol or vitamin D2 supplement were given according to our protocol based on the ranges of vitamin D deficiency as following: for mild deficiency (20 to less than 30 ng/mL) 60
000 unit/week&#44
for moderate deficiency (10 to less than 20 ng/mL) 80&#44
and for severe deficiency (less than 10 ng/mL) 10&#44
000 unit/week. Each vitamin D2 capsule contained 20&#44
000 units. The total dosage was divided into 2 separate doses giving on Monday and Friday.,The placebo and vitamin D2 capsules were made resemble and have the same weight.
Experimental Drug,Placebo Comparator Drug

Sponsors

No
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Thai male or female&#44; aged 18&#45;70 years old. 2. Chronic hepatitis C which was diagnosed more than 6 months. &#45; Albumin > 3.4 mg/dl &#45; Total bilirubin 75&#44;000 3. Compensated liver cirrhosis. 4. Consent for participation. 5. Serum 25 OH vitamin D level < 30 ng/ml.

Exclusion criteria

Exclusion criteria: 1. Underlying disease(s) ; Human Immunodeficiency virus (HIV) infection&#44; autoimmune disease. 2. Decompensated Liver Cirrhosis. 3. Pregnancy and/or lactating women. 4. Active viral or bacterial infection. 5. History of steroids or immunosuppressive therapy 6. No history of Pegylated interferons and interferons based therapies&#44; interferons withdrawal at least 6 months&#44; ingestion of drugs potentially capable of interacting with immune system

Design outcomes

Primary

MeasureTime frame
T&#45;Helper1/2 cytokines levels 6 weeks Cytokine quantitation was performed on bead&#45;based ELISA

Secondary

MeasureTime frame
IP&#45;10&#44;DPP&#45;4 levels 6 weeks quantitative sandwich enzyme immunoassay technique

Countries

Thailand

Contacts

Public ContactPiyawat Komolmit

MD&#44; M.Sc.

pkomolmit@yahoo.co.uk0906764824

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026