Predictors of Response to Combined Pegylated Interferon and Ribavirin in Chronic Hepatitis C Infected Egyptian Patients

NCT01758939 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 100000

Last updated 2013-04-17

No results posted yet for this study

Summary

Retrospective prospective cohort study aimed at Assessing the predictors to the response to the antiviral combined therapy with pegylated Interferon (Both types: Alfa 2 A and Alfa 2 B) in hepatitis C virus infected Egyptian patients.

Conditions

  • Hepatitis C, Chronic

Sponsors & Collaborators

  • Cairo University

    lead OTHER

Principal Investigators

  • Gamal Esmat, MD · Cairo University

  • Abdelrahman Zerki, PHD · Cairo University

  • Wahid Doss, MD · Cairo University

  • Maissa El Raziky, MD · Cairo University

  • Gamal Sheha, MD · Cairo University

  • Tarneem Darwish, MSc. · Cairo University

  • samy zaki, MD · Cairo University

  • Magdi El-Serafy, MD · Cairo Universty

  • Fathalla Sedky, MD · Cairo University

  • Ahmed M Nasr, MD · Cairo University

  • Mostafa Gabr, MD · Cairo University

  • Ali kassem, MD · Cairo University

  • Ibrahim Metawea, MD · Cairo University

  • Noaman Al-Garem, MD · Cairo University

  • Hassan Hamdy, MD · Cairo University

  • Tawheed Mwafy, MD · Cairo University

  • Khalil A Khalil, MD · Cairo University

  • Magdy Atta, MD · Cairo University

  • Osama E Salem, MD · Cairo University

  • Mohamed A Afify, MD · Cairo University

  • Mohamed S Al-Shazly, MD · Cairo University

  • Hamdy Mahfouz, MD · Cairo University

  • Mustafa Gabr, MD · Cairo University

  • Monquez Motaea, MD · Cairo University

  • Hossam Abdel-Latif, MD · Cairo University

Eligibility

Min Age
18 Years
Max Age
60 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-01-31
Primary Completion
2016-01-31
Completion
2017-01-31

Countries

  • Egypt

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01758939 on ClinicalTrials.gov