- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02798965
Prevalence of Circulating Parvovirus Genome in Recently Diagnosed Graves' Disease: a Case-control Study (GPCBasedow)
November 17, 2025 updated by: Centre Hospitalier Universitaire, Amiens
Lymphocytic thyroiditis is the most common autoimmune disease, usually affecting young women.
Although the aetiology and pathogenesis remain obscure, the most widely accepted hypothesis is an interaction between a genetic predisposition and an environmental trigger factor such as viral infection.
Parvovirus infections have been proposed as trigger factors for Hashimoto's thyroiditis and Graves' disease.
Study Overview
Study Type
Interventional
Enrollment (Actual)
52
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Amiens, France, 80054
- CHU Amiens
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 99 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- Graves' disease :patients treated for Graves' disease, the diagnosis date less than 4 months
- Control : patients cared for nodules or goiter
Exclusion Criteria:
- Patients undergoing immunosuppressive therapy including corticosteroids
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Basic Science
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Other: Control
patients with goiter or nodule
|
|
|
Experimental: Graves' disease
patients with Graves' disease
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
prevalence of circulating parvovirus genome
Time Frame: Day 0
|
Day 0
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Rachel DESAILLOUD, MD, PhD, CHU Amiens
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
General Publications
- https://www.em-consulte.com/article/753902/detection-de-levb19-parvovirus-b19-dans-les-thyroc
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
December 1, 2010
Primary Completion (Actual)
May 1, 2014
Study Completion (Actual)
May 1, 2014
Study Registration Dates
First Submitted
June 9, 2016
First Submitted That Met QC Criteria
June 9, 2016
First Posted (Estimated)
June 14, 2016
Study Record Updates
Last Update Posted (Estimated)
November 19, 2025
Last Update Submitted That Met QC Criteria
November 17, 2025
Last Verified
November 1, 2025
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
- Endocrine System Diseases
- Autoimmune Diseases
- Immune System Diseases
- Eye Diseases
- Exophthalmos
- Orbital Diseases
- Goiter
- Hyperthyroidism
- Thyroid Diseases
- Graves Disease
- Investigative Techniques
- Clinical Laboratory Techniques
- Diagnostic Techniques and Procedures
- Diagnosis
- Immunologic Techniques
- Immunologic Tests
- Serologic Tests
Other Study ID Numbers
- AOL10-DR-DESAILLOUD
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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