Impact of Metabolic Changes and Vitamin D Status on Virological Response in Patients With HCV Infection Treated by DAAs

HCV Clinical Trial

Official title:

Impact of Metabolic Changes and Vitamin D Status on Virological Response in Patients With Hepatitis C Viral Infection Treated by Direct Acting Antiviral Drugs

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT03820102
• Other study ID #: IR,VitD in HCV
• Status: Not yet recruiting
• Start date: March 2019
• Est. completion date: October 2019

Study information

• Verified date: February 2019
• Source: Assiut University
• Contact: Mohamed H Abdelgawad, specialist
• Phone: 01008778754
• Email: d_m_h_80[@]hotmail.com
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

1. Study Changes in lipid profile and the impact of Insulin resistance on virological response in patients with Hepatitis C viral infection treated by Direct Acting Antiviral agents

2. The assessment of serum vitamin D levels in HCV infected patients and predictive value of pre-treatment serum vitamin D level for achieving sustained virological response at 12 weeks post-treatment

Description:

Patients and methods:

This cross-sectional study will include 100patients of chronic HCV infection who attend El Raghy Assiut university Hospital, either inpatients or outpatients. Chronic HCV infection will be diagnosed based on detectable HCV RNA with anti-HCV Ab in patient with clinical and/or ultrasonographic criteria of chronic liver disease.

Patients will receive treatment to HCV by DAAs and follow up for 12 weeks to confirm sustained virological response

Method:

Patients presenting in this study will be subjected to the following:

1. Full history and clinical evaluation.

2. Body weight (kg) and height (m).

3. BMI will calculate as weight divided by squared height (kg/m2).

4. Waist circumference will measured at a level midway between the lowest rib and the iliac crest, and the hip circumference at the level of the great trochanters, with the legs close together.

5. Blood pressure (mmHg) was measured twice in the upper arm after a 10-min period of rest and taken an average.

Laboratory investigations will include:

• Complete blood count (CBC)

• Liver function test

• HCV Ab and HCV RNA by PCR

• HBs Ag

• Alpha fetoprotein

• Lipid profile

• Serum urea and creatinine

• Fasting blood sugar (FBG)and Serum fasting insulin level

• Insulin resistance determined via Homeostasis Model Assessment (HOMA-IR) IR = fasting insulin (µu/ml) × fasting glucose (mmol/L) ----------------------------------------------------------------- 22.5 An index value of ˃ 2. 5 was defined as IR (Huang et al., 2011)

• Vitamin D level:

Vitamin D deficiency wasdefined as a 25 (OH)-vitamin D serum level < 20 ng/mL, vitaminD insufficiency as 25 (OH)-vitamin D levels of 20 - 29.9ng/mL, and normal vitamin D levels ≥ 30 ng/mL (Holick MF et al.,2011)

• Abdominal Ultrasound

• Electrocardiogram (ECG)

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 100
• Est. completion date: October 2019
• Est. primary completion date: September 2019
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Chronic HCV will receive DAAs for treatment

Exclusion Criteria:

1. Decompensated liver cirrhosis, hepatocellular carcinoma, history of liver transplant

2. Co-existing liver disease (hepatitis B virus, autoimmune hepatitis, human immunodeficiency virus)

3. Extra-hepatic malignancy except after two years of disease free interval.

4. Patients with diabetes mellitus.

5. Patients with Chronic kidney disease.

6. Pregnancy or in ability to use effective contraception.

7. Patients with history of using lipid lowering therapy

8. relapser or failure of previous HCV treatment

Related Conditions & MeSH terms

• HCV

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
Assiut University

References & Publications (3)

Janovy J Jr. Problems in the comparative physiology of some trypanosomatid flagellates. Acta Trop. 1977 Jun;34(2):177-84. — View Citation

Ramachandran N, Colman RF. Evidence for a critical glutamyl and an aspartyl residue in the function of pig heart diphosphopyridine nucleotide dependent isocitrate dehydrogenase. Biochemistry. 1977 Apr 19;16(8):1564-73. — View Citation

Selhub J, Rosenberg IH. Demonstration of high-affinity folate binding activity associated with the brush border membranes of rat kidney. Proc Natl Acad Sci U S A. 1978 Jul;75(7):3090-3. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	SVR12	sustained virological response 12 week after treatment	12 week after treatment