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Pathogeny Exploration and Treatment Optimization for Refractory Vitiligo

Pathogeny Exploration and Treatment Optimization for Refractory Vitiligo

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IPR-16009964
Enrollment
Unknown
Registered
2016-11-22
Start date
2017-01-01
Completion date
Unknown
Last updated
2017-04-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

vitiligo

Interventions

Minocycline Group:oral Minocycline
Glucocorticoid Group:oral Minocycline
Simvastatin Group:oral Simvastatin
Placebo Group:oral Placebo

Sponsors

Shanghai Dermatology Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18 to 70 years old; 2. identify vitiligo; 3. Above, a history of more than 1 year, in the course of the disease at least taken: (1) local external use potent corticosteroids; (2) system application of glucocorticoid hormone; (3) PUVA; (4) narrow wave ultraviolet ray; (5) 308 excimer laser; (6) melanin cell transplantation, two or more treatments; 4. Not used any treatment could impact the present study before recruitment; 5. no serious liver and kidney and blood system diseases; 6. the patients agree to and sign the informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients in progressive stage: severe heart renal insufficiency, diabetes, high blood pressure, tuberculosis, and hepatitis b and other infectious diseases; 2. Patients with plateau: have scar constitution; 3. With severe mental illness, do not have independent ability; 4. the test drug allergy or intolerance; 5. Pregnancy or breast-feeding women, or ready to pregnant women; 6. In recent 3 months, participated in other clinical trials; 7. Any medical history, according to the researchers may interfere with the test results or increase the risk of the subjects; 8. compliance is bad, not strictly carry out the plan.

Design outcomes

Primary

MeasureTime frame
size of lesion;

Countries

China

Contacts

Public ContactYeqiang Liu

Shanghai Dermatology Hospital

lyqdoctor@163.com+86 18017336841

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026