Clinical Trials Logo

Clinical Trial Summary

Primary Purpose:

1. Evaluate the prevalence and incidence of HEV infection in MHD patients.

2. Compare differences of the prevalence and incidence between the MHD patients and the control. .

Secondary purpose:

Analyze risk factors of HEV infection.


Clinical Trial Description

This is an Epidemiological study manufactured by Xiamen University. The primary purpose of this study is to evaluate the prevalence and incidence of HEV infection in MHD patients and to compare differences between the MHD patients and the control. The secondary purpose of this study is to analyze risk factors of the infection of HEV. There are two phases in this study. The first phase is a cross-sectional study. Approximately 200 MHD patients will be enrolled in MHD patient group, followed by control group's enrollment according to the age and gender of the MHD patient group. Blood samples and questionnaire were got at this time. Secondly, 100 enrolled volunteers in each group who is negative for HEV-IgM、HEV-IgG、HEV RNA will be introduced into the cohort study. The MHD patient group will been taken blood samples at an interval of 3 month until the 12th month after the first phase, however, the control group only need one blood sample at 12th month. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02645955
Study type Observational [Patient Registry]
Source Xiamen University
Contact
Status Completed
Phase
Start date May 2016
Completion date March 2018

See also
  Status Clinical Trial Phase
Active, not recruiting NCT05415345 - Immunogenicity and Safety of Co-immunization With Cecolin and Hecolin Phase 4
Recruiting NCT05300425 - Seroprevalence of Leptospirosis in Val Müstair, Switzerland
Not yet recruiting NCT06306196 - Immunogenicity and Safety of Hecolin® in HIV Positive/Negative Adults and in Children Phase 2