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Effect of camel milk on chronic hepatitis C

investigating the effects of Camel Milk Products on the laboratory markers in the patients with chronic hepatitis, genotype 2 & 3

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT2013112515533N1
Enrollment
40
Registered
2014-08-20
Start date
2014-07-23
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Chronic hepatitis C. Chronic viral hepatitis C

Interventions

Intervention 1: Intervention group: Pegah interferon (Pgasys) at a dose of 180 mcg subcutaneously once weekly, and ribavirin dose of 800 to 1200 mg based on body weight orally daily and camel milk 250
Treatment - Drugs
Intervention group: Pegah interferon (Pgasys) at a dose of 180 mcg subcutaneously once weekly, and ribavirin dose of 800 to 1200 mg based on body weight orally daily and camel milk 250 cc daily in the
Control group: Pegah interferon (Pgasys) at a dose of 180 mcg subcutaneously once weekly, and ribavirin dose of 800 to 1200 mg based on body weight orally for three months.

Sponsors

Mashhad University of Medical Sciences ,Vice chancellor for research
Lead Sponsor
Razi vaccine and Serum research Institue of Mashhd
Collaborator

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: inclusion criteria: age 18 to 70 years? the detection of serum HCV RNA by PCR. exclusion criteria:Decompensated cirrhosis; autoimmune diseases; cancer; infected with HIVorHBV;neutropenia;thrombocytopenia; creatinine higher;organ transplant;severe heart disease; chronic lung disease; uncontrolled psychiatric illness; epilepsy; diabetic retinopathy; active alcohol or addiction; pregnancy;anemia;non-compliance with the prescribed dosage milk; discourage patients from continuing to participate in the plan; other genotypesto participate in the plan; other genotypes

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Quantification of HCV RNA. Timepoint: One Month. Method of measurement: PCR.;Level of ALT,AST. Timepoint: One Month. Method of measurement: unit /ml.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMohammadreza Noras

Faculty of Traditional Medicine

norasmr901@mums.ac.ir+98 51 3855 2189

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026