Role OF OCT-A TO Detect Possible Retinal Vascular Complications of Sofosbuvir in Patients With Hepatitis C

Sponsor
Mohamed Saad (Other)
Overall Status
Unknown status
CT.gov ID
NCT04159246
Collaborator
(none)
30
1
9.6
3.1

Study Details

Study Description

Brief Summary

The purpose of this study is to prospectively evaluate the value of Optical coherence tomography angiography (OCT-A) for the of detection of suspected retinal complications With Sofosbuvir (Sovaldi) in Patients With Hepatitis C Virus Infection

Condition or Disease Intervention/Treatment Phase
  • Device: Optical coherence tomography angiography
  • Drug: Sofosbuvir (Sovaldi)

Detailed Description

During 3 months duration ( the treatment course duration) , Optical coherence tomography angiography (OCT-A) will be performed to 30 eyes of 30 patients with a documented diagnosis of chronic hepatitis C before and after receiving dual-therapy planning (Daclatasvir - Sofosbuvir (Sovaldi)) , normal renal functions And Rheumatoid factor tests , will undergo a comprehensive ophthalmic examination including:

  • Manifest refraction

  • Corrected distance visual acuity

  • Anterior segment examination using slit lamp and tear film breakup time test

  • Fundus examination

Recent Optical coherence tomography angiography (OCT-A) will be performed to all patients before Treatment Administration.

Examination will be performed using "Optovue AngioVue®" "Optovue, Inc., Fremont, CA", which uses split-spectrum amplitude-decorrelation angiography algorithm, which minimizes motion noise. This system also allows quantitative analysis, since it provides numerical data about flow area and flow density maps.

The patient will be examined before and after finishing the treatment course

  • Optical coherence tomography angiography (OCT-A) image acquisition OCT-A will be done for all patients who are instructed to focus on a fixation target. OCTA images are obtained using the "RTVue XR Avanti (AngioVue; Optovue Inc, Fremont, California, USA)" machine and the incorporated "AngioVue OCT-A" system. Algorithm used is Split-Spectrum Amplitude Decorrelation Algorithm (SSADA). The scans which will be included in the study are of high signal strength more than 0.7 and they will be carefully inspected for motion artifacts. Automatic segmentation of intraretinal layers will be done using the automated software of the machine (version 2016.2.0; Optovue Inc). Angio-retina scan sizes in this study will be 6 X 6 mm for all eyes. Assessment of the macular vessel density will be done for superficial vascular layer, capillary plexus, deep capillary plexus and all retinal plexuses). Assessment of the foveal avascular zone on both superficial vascular layer (SVL) and deep capillary plexuses (DCP); including its size, perimeter and circularity (regularity) index. Circularity index is a measure of compactness of a shape relative to a circle. The circularity index of a circle is 1.0. Thus, a ratio closer to 0 indicates an irregular shape, and that closer to 1.0 indicates a circular shape.

All results will be in numerical values (percentage) to compare retinal vascularity before and after using the drug. Best corrected visual acuity (in values from o.o5 to 1.0) , dryness (in seconds) will be also measured before and after drug administration and it will be compared .

Study Design

Study Type:
Observational
Anticipated Enrollment :
30 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Role OF OCT-A TO Detect Possible Retinal Vascular Complications of Sofosbuvir (Sovaldi) in Patients With Hepatitis C Virus Infection
Actual Study Start Date :
Feb 10, 2019
Anticipated Primary Completion Date :
Nov 30, 2019
Anticipated Study Completion Date :
Nov 30, 2019

Arms and Interventions

Arm Intervention/Treatment
Sovaldi group

patients with a documented diagnosis of chronic hepatitis C , normal renal functions And Rheumatoid factor tests (to exclude Purtscher like retinopathy as a rare presentation of cryoglobuinemia which considered one of extra hepatic manifestations of HCV)

Device: Optical coherence tomography angiography
Recent Optical coherence tomography angiography "OCT-A" will be performed to all patients before Treatment Administration. Examination will be performed using Optovue AngioVue® "Optovue, Inc., Fremont, CA", which uses split-spectrum amplitude-decorrelation angiography algorithm, which minimizes motion noise. This system also allows quantitative analysis, since it provides numerical data about flow area and flow density maps. The patient will be examined before and after finishing the treatment course
Other Names:
  • OCTA
  • Drug: Sofosbuvir (Sovaldi)
    Sofosbuvir (tradename Sovaldi) is a direct acting antiviral medication used as part of combination therapy to treat chronic Hepatitis C , here it's used with Daclatasvir for 3 months
    Other Names:
  • Sovaldi
  • Outcome Measures

    Primary Outcome Measures

    1. Assessment percentage of change in macular vessels density using OCTA [3 months]

      Evaluate the suspected retinal vascular complications With Sofosbuvir (Sovaldi) ) in Patients With Hepatitis C Virus Infection, All results will be in numerical values (percentage) to compare retinal vascularity before and after using the drug..

    2. visual acuity changes with Sofosbuvir [3 months]

      Comparing best corrected visual acuity (in values from o.o5 to 1.0) before and after drug administration .

    Secondary Outcome Measures

    1. amount of ocular dryness with Sofosbuvir using tear up breaking test [3 months]

      Measuring amount of ocular dryness using Tear-up breaking test, dryness will be evaluated in seconds before and after drug administration and it will be compared .

    2. Role of Optical coherence tomography angiography (OCTA) in detection early signs retinopathy depending on changes in vascular density [3 months]

      Confirm the advantages of Optical coherence tomography angiography (OCT - A) in detection early signs retinopathy depending on changes in vascular density (evaluated as a percentage)

    3. amount of ocular dryness with Sofosbuvir using Schirmer's [3 months]

      Measuring amount of ocular dryness using Tear-up breaking test, dryness will be evaluated in millimeters of wetness of schirmer's strips before and after drug administration and it will be compared .

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    20 Years to 80 Years
    Sexes Eligible for Study:
    All
    Inclusion Criteria:
    • Age between 20 and 80 years.

    • Patients with chronic hepatitis C enrolled for (Daclatasvir - Sofosbuvir (Sovaldi)) .

    • Patients who have normal ocular and fundoscopic examination before the onset of treatment.

    Exclusion Criteria:
    • Relapsed cases who have formerly taken the antiviral therapy (depending on the basis of medical record and filing system), or treated with interferon for any other cause .

    • Patients with elevated renal functions or positive Rheumatoid factor (as a clue to diagnose Purtscher like retinopathy which is a rare presentation of cryoglobulinemia ,considered one of extra hepatic manifestations of HCV )

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Cairo University - Kasr Alainy Cairo Egypt

    Sponsors and Collaborators

    • Mohamed Saad

    Investigators

    • Principal Investigator: Hany E Elmekewy, MD, Cairo University
    • Principal Investigator: Magada S Abdelaziz, MD, Cairo University
    • Principal Investigator: Yomna A Abdelwahab, MD, Cairo University
    • Study Chair: Mai I Mehrez, MD, National Hepatology & Tropical Medicine Research Institute

    Study Documents (Full-Text)

    More Information

    Publications

    Responsible Party:
    Mohamed Saad, Resident of Ophthalmology , Cairo University - researcher, Cairo University
    ClinicalTrials.gov Identifier:
    NCT04159246
    Other Study ID Numbers:
    • s-5-2019
    First Posted:
    Nov 12, 2019
    Last Update Posted:
    Nov 12, 2019
    Last Verified:
    Nov 1, 2019
    Individual Participant Data (IPD) Sharing Statement:
    Yes
    Plan to Share IPD:
    Yes
    Studies a U.S. FDA-regulated Drug Product:
    Yes
    Studies a U.S. FDA-regulated Device Product:
    Yes
    Product Manufactured in and Exported from the U.S.:
    Yes
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Nov 12, 2019