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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02642822
Other study ID # CMV-EPI-002
Secondary ID
Status Completed
Phase N/A
First received December 24, 2015
Last updated July 13, 2016
Start date October 2014
Est. completion date April 2016

Study information

Verified date December 2015
Source Xiamen University
Contact n/a
Is FDA regulated No
Health authority China: Ministry of Science and Technology
Study type Observational

Clinical Trial Summary

In this study, 100 female students aged 18 to 30 years old in Xiamen University will be enrolled. On the first visit, blood, saliva and urine samples of all participants will be collected. Then saliva and urine samples will be collected at two-week interval until 6 months. Serum samples will be tested the PP150-IgG titer. Saliva and urine samples will be used to test CMV DNA by PCR. The primary purpose of this study is to identify the relationship between baseline PP150-IgG titer and CMV infection.


Recruitment information / eligibility

Status Completed
Enrollment 102
Est. completion date April 2016
Est. primary completion date April 2016
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 30 Years
Eligibility Inclusion Criteria:

- 18-30 years old

- female students of Xiamen University

Exclusion Criteria:

- students who have the serious diseases

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
China School of public health of Xiamen University Xiamen Fujian

Sponsors (1)

Lead Sponsor Collaborator
Jun Zhang

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary rate of active CMV infection in different PP150-IgG titer 1 year No
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