Metabolic Changes in Chronic HCV Patients Receiving DAAS

NCT ID: NCT04211844

Last Updated: 2020-01-02

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Total Enrollment

100 participants

Study Classification

OBSERVATIONAL

Study Start Date

2019-10-01

Study Completion Date

2020-04-30

Brief Summary

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Observational Study to check metabolic changes between two different hepatitis C antiviral medication groups. This study will evaluate the impact of different treatments on Serum lipid changes, fasting blood glucose and glycated hemoglobin . It will determine if changes are due to different Antiviral regimens or due to different Sustained virological response rates.

Detailed Description

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The aim of this study is;

* To investigate and compare the changes in the total lipid profile and glycated hemoglobin (HbA1c) for chronic hepatitis C patients after receiving either one of two different direct antiviral regimens: sofosbuvir/daclatasvir and sofosbuvir/ledipasvir (Harvoni).
* To evaluate the impact of treatment response on the serial changes of serum lipid levels and glycated hemoglobin after receiving either of the two different direct antiviral regimens.
* To determine whether the change in the lipid profile and HbA1C is due to different antiviral regimens or due to different SVR rates.

Recruitment will be based on reviewing newly admitted patients and choosing those who are treatment naive and easy to treat according to study inclusion criteria. Thorough check of patient file will be done before starting the study. Eligible patients will sign a consent before starting both the treatment and the study. Patients will be divided into two groups taking treatment for 12 weeks. After treatment, patients will be followed-up for up to 12 weeks.

Patients will be asked to fast for a total of 12 hours. First 8 hours of fasting, a blood sample will be withdrawn for fasting blood sugar and glycated hemoglobin. At 12 hours of fasting, another sample will be withdrawn for lipid profile.

At baseline, patients dermographics (sex, age, weight, height, BMI), full medication history and full medical history will be collected from both patient file and patient consultation. After end of treatment at week 24, weight will be measured and BMI will be also be calculated. Adverse effects reporting:Patients will be asked about any undesirable effects detected throughout the trial which would be reported.

For the whole study period, patients will be subjected to assessment of the following:

* CBC, ALT, AST, total serum bilirubin, and creatinine will be done every 4 weeks (week 0, 4, 8, 12, 16, and 24)
* Complete lipid profile, fasting blood glucose, and HbA1c levels at baseline, during therapy (week 4), and at week 24 after discontinuation of therapy.
* Quantitative PCR for HCV RNA at week 0 and 24.

Results will be collected and tabulated in excel sheet to undergo statistical analysis. Statistical analyses will be done using the SPSS software (Statistical Package for the Social Sciences). Proportions will be compared using Fisher's exact test and means will be compared with Student's t-test or Wilcoxon rank sum test, where appropriate.

Conditions

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Chronic Hepatitis C

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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sofosbuvir plus daclatasvir

50 patients receiving 400 mg sofosbuvir plus daclatasvir 60 mg once daily for 12 weeks. Blood samples are taken at baseline (week 0), week 4 (during treatment) and week 24 (post treatment after discontinuation of treatment at sustained virological response). Samples will be evaluated for lipid profiles, fasting blood sugar and glycated hemoglobin.

sofosbuvir plus daclatasvir

Intervention Type DRUG

50 patients in the first group will receive 400 mg sofosbuvir plus daclatasvir 60 mg once daily for 12 weeks.

sofosbuvir plus ledipasvir

50 patients receiving 400 mg sofosbuvir plus ledipasvir 90 mg (Harvoni) once daily for 12 weeks. Blood samples are taken at baseline (week 0), week 4 (during treatment) and week 24 (post treatment after discontinuation of treatment at sustained virological response). Samples will be evaluated for lipid profiles, fasting blood sugar and glycated hemoglobin.

Sofosbuvir plus Ledipasvir

Intervention Type DRUG

50 patients in the second group will receive 400 mg sofosbuvir plus ledipasvir 90 mg (Harvoni) once daily for 12 weeks.

Interventions

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sofosbuvir plus daclatasvir

50 patients in the first group will receive 400 mg sofosbuvir plus daclatasvir 60 mg once daily for 12 weeks.

Intervention Type DRUG

Sofosbuvir plus Ledipasvir

50 patients in the second group will receive 400 mg sofosbuvir plus ledipasvir 90 mg (Harvoni) once daily for 12 weeks.

Intervention Type DRUG

Other Intervention Names

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Sovaldi Daklinza Harvoni

Eligibility Criteria

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Inclusion Criteria

* Male or female patients age 18 to 75 years old. Patients ≥ 65 years old should undergo cardiological assessment prior to therapy by ECG, echocardiography and cardiological consultaion.
* Easy to treat group: treatment naïve patients with serum HCV RNA positivity by PCR.
* Clinically stable condition.
* Platelet count ≥ 150,000/mm³.
* INR ≤ 1.2
* Serum albumin ≥ 3.5 g/dl.
* Total serum bilirubin ≤ 1.2 mg/dl.
* eGFR \> 30 ml/min

Exclusion Criteria

* Pregnancy or inability to use effective contraceptives.
* Inadequately controlled diabetes mellitus (HbA1c \> 9%)
* HCV-HIV co infection.
* HBV-HCV co infection.
* Any cause for chronic liver disease other than hepatitis C
* Hyper or hypothyroidism.
* Hepatocellular carcinoma, except 6 months after intervention aiming at cure with no evidence of activity by dynamic imaging (CT or MRI)
* Extra-hepatic malignancy except after two years of disease-free interval.
* Fibrosis: FIB-4 index ≥ 3
* Patients prescribed with lipid-lowering agents (statins).
Minimum Eligible Age

18 Years

Maximum Eligible Age

75 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Ain Shams University

OTHER

Sponsor Role lead

Responsible Party

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Nehal Khaled Abdel Raouf Abdel Fattah

Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Nehal Abdel Fattah, PharmB

Role: PRINCIPAL_INVESTIGATOR

Ain Shams University

Locations

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El Demerdash Hospital

Cairo, Abbasseya, Egypt

Site Status RECRUITING

Countries

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Egypt

Central Contacts

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Nehal Abdel Fattah, PharmB

Role: CONTACT

+201065600196

Sara Zaki, PhD

Role: CONTACT

+201008742248

Facility Contacts

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Nehal Abdel Fattah, pharmB

Role: primary

+201065600196

Other Identifiers

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164

Identifier Type: -

Identifier Source: org_study_id

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