Correlation of Glucose and Lipid Metabolism Levels With Vitiligo
NCT ID: NCT05968235
Last Updated: 2023-08-01
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
963 participants
OBSERVATIONAL
2020-02-01
2023-03-25
Brief Summary
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Detailed Description
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This study intends to conduct a cross-sectional study, using questionnaires to collect and register vitiligo patients' disease information, etc., to establish a database of study subjects, and to collect peripheral blood samples from vitiligo patients to test the levels of key indicators of glycolipid and lipid metabolism, and to analyze their correlation with clinical features, disease activity, and treatment of vitiligo. Through the above studies, clinical evidence for the involvement of abnormalities in glycolipid and lipid metabolism in the development of vitiligo was provided.
Conditions
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Study Design
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CASE_CONTROL
CROSS_SECTIONAL
Study Groups
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Vitiligo
Patients diagnosed with vitiligo
Collecting blood samples
Peripheral blood was collected from the study subjects and blood glucose, glycosylated hemoglobin, triglycerides, total cholesterol, high-density lipoprotein and low-density lipoprotein levels were measured in the peripheral blood.
Healthy
Healthy volunteers with sex- and age-matched with vitiligo patients
Collecting blood samples
Peripheral blood was collected from the study subjects and blood glucose, glycosylated hemoglobin, triglycerides, total cholesterol, high-density lipoprotein and low-density lipoprotein levels were measured in the peripheral blood.
Interventions
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Collecting blood samples
Peripheral blood was collected from the study subjects and blood glucose, glycosylated hemoglobin, triglycerides, total cholesterol, high-density lipoprotein and low-density lipoprotein levels were measured in the peripheral blood.
Eligibility Criteria
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Inclusion Criteria
2. Male or female subjects, age between 18 and 60 years old;
3. Stable vital signs;
4. Study subjects voluntarily signed an informed consent form.
Exclusion Criteria
2. Women who are pregnant or breastfeeding shall be asked and determined by a clinician;
3. Subjects who suffer from psychiatric disorders, etc. and who are not capable of cooperating with the follow-up study shall be asked and determined by a clinician.
18 Years
60 Years
ALL
Yes
Sponsors
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Xijing Hospital
OTHER
Responsible Party
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Li Chunying-1
Vice Chief
Principal Investigators
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Chunying Li
Role: PRINCIPAL_INVESTIGATOR
Air Force Military Medical University, China
Locations
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Xijing Hospital
Xi'an, Shaanxi, China
Countries
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Other Identifiers
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XJPF-LCY-V202307
Identifier Type: -
Identifier Source: org_study_id
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