CClinicalTrials.gg
CompletedNCT05968235Updated Aug 1, 2023

Correlation of Glucose and Lipid Metabolism Levels With Vitiligo

An observational study in Metabolism Disorder, Glucose, Metabolism Disorder, Lipid and Vitiligo, sponsored by Xijing Hospital. Completed at 1 site in China. Open to participants aged 18 Years to 60 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2023-08-01.

Sponsored by Xijing Hospital · Observational

Study type
Observational
Model
Case-control
Time perspective
Cross-sectional
Enrollment
963
Ages
18 Years to 60 Years
Sex
All
01

Study summary

The goal of this observational study is to compare serum glucose and lipid metabolism levels between health volunteers and vitiligo patients. The main question it aims to answer is whether vitiligo is related to glucose and lipid metabolism disorders. Participants will complete a vitiligo questionnaire and test serum levels of indicators related to glucose and lipid metabolism. Researchers will compare vitiligo patients with healthy volunteers to see if there is a correlation between vitiligo and disorders of glucose and lipid metabolism.

Read the detailed description

Vitiligo is a common autoimmune skin disease, which causes white spot formation due to destruction of epidermal melanocytes, severely affecting the physical and mental health of patients, but treatment is extremely difficult due to unclear pathogenesis. Studies have reported that patients with type I diabetes mellitus combined with vitiligo, the risk of metabolic syndrome, diabetes mellitus, elevated lipids, and obesity in vitiligo patients is higher than that of healthy controls, and other studies have reported that vitiligo lesions in patients with hypercholesterolemia combined with vitiligo treated with simvastatin get rapid skin color, suggesting that there is a correlation between glucose and lipid metabolism and the vitiligo disease, but as of now there is no research study on the correlation of glucose and lipid metabolism and vitiligo pathogenesis, much less large data can be analyzed for reference. Therefore, there is an urgent need to study the metabolic profile of vitiligo patients and utilize the basic research platform to explore the role of abnormal body metabolism in the onset or progression of vitiligo.

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.

02

Conditions studied

  • Metabolism Disorder, Glucose
  • Metabolism Disorder, Lipid
  • Vitiligo

Keywords

  • Vitiligo
  • Glucose
  • Lipid
03

In context

Vitiligo

298 studies on the registry are indexed under Vitiligo; 69 are open to participants now.

This study's enrollment of 963 is above the median of 111 across 60 observational studies indexed under Vitiligo.

Browse Vitiligo studies →

Lead sponsor

Xijing Hospital is the lead sponsor of 465 studies on the registry; 157 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 60 Years
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Probability sample

Study population

We recruited patients with clinically diagnosed vitiligo and age- and sex-matched healthy volunteers.

Inclusion criteria

  1. Patients diagnosed as vitiligo by a dermatologist based on a combination of clinical manifestations (milky white or porcelain white patches), Wood's Lamp test results (bright white fluorescence), and histopathologic test results (reduction or disappearance of epidermal melanocytes in the white patches);
  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

Exclusion Criteria:

  1. Subjects who have been systematically using glucocorticoids, immunosuppressants, etc. that affect glycolipid levels due to a combination of diseases other than metabolic diseases in the last 3 months shall be asked and determined by a clinician;
  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.
05

Study design

Observational model
Case-control
Time perspective
Cross-sectional
Enrollment
963 participants (actual)
Target follow-up
1 Year
Patient registry
Yes
Biospecimen retention
Samples with dna

Groups and cohorts

  • Vitiligo

    Patients diagnosed with vitiligo

    Other: Collecting blood samples

  • Healthy

    Healthy volunteers with sex- and age-matched with vitiligo patients

    Other: Collecting blood samples

Interventions

  • OtherCollecting 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.

06

What researchers measure

Primary outcomes

  1. Demographic and epidemiological information of the study subjects

    Detailed records of demographic information (age, gender, occupation, education degree, life history, et al.), clinical information of vitiligo (age at onset, duration, severity, type, treatment, complication, et al.) and physical examination index (height, weight, blood pressure, heart rate).

    Time frame: 2020.02.01-2023.03.25

  2. Serum glucose and lipid metabolism levels of the study subjects

    Detection of fasting blood glucose, glycosylated hemoglobin, triglycerides, total cholesterol, high-density lipoproteins, and low-density lipoproteins in peripheral blood of study subjects.

    Time frame: 2020.02.01-2023.03.25

07

Study locations

1 site
  • Xijing Hospital
    Xi'an, Shaanxi 710032, China
08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 1, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05968235
Lead sponsor
Xijing Hospital
Responsible party
Li Chunying-1 (Vice Chief, Xijing Hospital) — Principal investigator
First posted
Aug 1, 2023
Start date
Feb 1, 2020
Primary completion
Mar 25, 2022
Completion
Mar 25, 2023
Last update
Aug 1, 2023

Study contacts

Chunying Li
principal investigator · Air Force Military Medical University, China

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Jul 2023. You cannot join it, but the record below documents what was studied.

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