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Multi-center Registration Study of Adult Onset Still's Disease in Chinese Population (MAOSDC)

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT03651193
Recruitment Status : Recruiting
First Posted : August 29, 2018
Last Update Posted : February 2, 2021
Sponsor:
Information provided by (Responsible Party):
Qianjin Lu, MD, PhD, Second Xiangya Hospital of Central South University

Brief Summary:
This multi-center registration study will investigate the clinical characteristics of AOSD population in China , identify possible factors inducing the onset and active condition of AOSD in Chinese population , and identify the new high specific and sensitive markers of AOSD

Condition or disease Intervention/treatment
Adult Onset Still Disease Diagnostic Test: Exon sequencing and Methylated sequencing

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Study Type : Observational
Estimated Enrollment : 150 participants
Observational Model: Cohort
Time Perspective: Cross-Sectional
Official Title: Multi-center Registration Study of Adult Onset Still's Disease in Chinese Population
Actual Study Start Date : November 28, 2018
Estimated Primary Completion Date : June 30, 2022
Estimated Study Completion Date : December 31, 2022


Group/Cohort Intervention/treatment
AOSD
Patients fulfill Japan's Yamaguch AOSD classification
Diagnostic Test: Exon sequencing and Methylated sequencing
Exon sequencing and Methylated sequencing

Control
Use 1:1 group matching, should meet the following condition -s : same gender as matching case; same age as matching case or the difference ranges within 1 year; no Immune related diseases (e.g. Psor -iasis, Systemic Lupus Erythematos -us, Dermatomyositis, Scleroderma, Rheumatoid Arthritis, Type 1 Diabet -es, Behcet's disease, Sjogren's Syndrome, Hyperthyroidism, etc.); no family history of immune related diseases.
Diagnostic Test: Exon sequencing and Methylated sequencing
Exon sequencing and Methylated sequencing




Primary Outcome Measures :
  1. gene expression level and methylation level [ Time Frame: 0 day ]

    The data of this study is managed by the Hunan Key Laboratory of Medical Epigenomics (Department of Dermatology, The Second Xiangya Hospital of Central South University). The authenticity, integrity and confidentiality of clinical data are required to be ensured, original case and case report form shall be filled out by investigator or the designated person of researcher and shall not be altered at will. If necessary, the name of the changer and the date of modification should be signed.

    Statistical analysis will use GraphPad Prism or SPSS software. All statistical tests will be performed using a two-sided test, P values less than 0.05 will be considered statistically significant, the confidence interval uses 95%. The measurement data will be statistically described using mean ± standard deviation or median (minimum, maximum). Disease exposure factors and impact analysis will be based on descriptive statistical analysis.



Biospecimen Retention:   Samples With DNA
whole blood 5ml,serum 1.5ml


Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Sampling Method:   Probability Sample
Study Population
Chinese population
Criteria

Inclusion Criteria:

  • AOSD: Patients fulfill Japan's Yamaguch AOSD classification.
  • Control: Use 1:1 group matching, should meet the following condition -s : same gender as matching case; same age as matching case or the difference ranges within 1 year; no Immune related diseases (e.g. Psor -iasis, Systemic Lupus Erythematos -us, Dermatomyositis, Scleroderma, Rheumatoid Arthritis, Type 1 Diabet -es, Behcet's disease, Sjogren's Syndrome, Hyperthyroidism, etc.); no family history of immune related diseases.

Exclusion Criteria:

  • Anyone with physical or mental illness that may affect the assessment will be excluded, such as patients with hearing or speech expression disorders.

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03651193


Contacts
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Contact: Qianjin Lu, MD,PHD +86-13787097676 qianlu5860@gmail.com
Contact: Yuwei Li, MD +86-15200854262 yuweili@csu.edu.cn

Locations
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China, Changsha
The Second Xiangya Hospital of Central South University Recruiting
Hunan, Changsha, China, 410011
Contact: Xiangqi Tang, MD, PhD    +86-731-84896038    xiangyagcp@126.com   
Principal Investigator: Qianjin Lu, MD, PhD         
Sub-Investigator: Yuwei Li, MD         
Sponsors and Collaborators
Second Xiangya Hospital of Central South University
Investigators
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Principal Investigator: Qianjin Lu, MD,PHD Central South University
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Responsible Party: Qianjin Lu, MD, PhD, Professor and Director, Dept. of Dermatology, The Second Xiangya Hospital of Central South University, Second Xiangya Hospital of Central South University
ClinicalTrials.gov Identifier: NCT03651193    
Other Study ID Numbers: MAOSDC20180720
First Posted: August 29, 2018    Key Record Dates
Last Update Posted: February 2, 2021
Last Verified: January 2021
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Keywords provided by Qianjin Lu, MD, PhD, Second Xiangya Hospital of Central South University:
Adult Onset Still's Disease
Chinese population
Additional relevant MeSH terms:
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Arthritis, Juvenile
Still's Disease, Adult-Onset
Arthritis
Joint Diseases
Musculoskeletal Diseases
Rheumatic Diseases
Connective Tissue Diseases
Autoimmune Diseases
Immune System Diseases
Arthritis, Rheumatoid