Multi-center Registration Study of Adult Onset Still's Disease in Chinese Population (MAOSDC)
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| ClinicalTrials.gov Identifier: NCT03651193 |
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Recruitment Status :
Recruiting
First Posted : August 29, 2018
Last Update Posted : February 2, 2021
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| Condition or disease | Intervention/treatment |
|---|---|
| Adult Onset Still Disease | Diagnostic Test: Exon sequencing and Methylated sequencing |
Show detailed description
| 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 |
|---|---|
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AOSD
Patients fulfill Japan's Yamaguch AOSD classification
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Diagnostic Test: Exon sequencing and Methylated sequencing
Exon sequencing and Methylated sequencing |
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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.
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Diagnostic Test: Exon sequencing and Methylated sequencing
Exon sequencing and Methylated sequencing |
- 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
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.
| Ages Eligible for Study: | 18 Years and older (Adult, Older Adult) |
| Sexes Eligible for Study: | All |
| Accepts Healthy Volunteers: | Yes |
| Sampling Method: | Probability Sample |
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.
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
| Contact: Qianjin Lu, MD,PHD | +86-13787097676 | qianlu5860@gmail.com | |
| Contact: Yuwei Li, MD | +86-15200854262 | yuweili@csu.edu.cn |
| 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 | |
| Principal Investigator: | Qianjin Lu, MD,PHD | Central South University |
| 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 |
| Studies a U.S. FDA-regulated Drug Product: | No |
| Studies a U.S. FDA-regulated Device Product: | No |
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Adult Onset Still's Disease Chinese population |
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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 |

