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Dot matrix laser + Betamethason Copound Injection / Triamcinolone Acetonide + NB-UVB vs dipropionate betamethasone cream + NB-UVB for the treatment of the acral type (including the subcarinal parts) of vitiligo: the efficacy and safety of the multi-center, open, randomized controlled clinical trials

Dot matrix laser + Betamethason Copound Injection / Triamcinolone Acetonide + NB-UVB vs dipropionate betamethasone cream + NB-UVB for the treatment of the acral type (including the subcarinal parts) of vitiligo: the efficacy and safety of the multi-center, open, randomized controlled clinical trials

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-12002593
Enrollment
Unknown
Registered
2014-09-12
Start date
2012-09-01
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

test group:lattice Laser + compound betamethasone injection / triamcinolone acetonide injection + NB-UVB
control group:Betamethasone cream + NB-UVB

Sponsors

The First Hospital of China Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
14 Years to 65 Years

Inclusion criteria

Inclusion criteria: (1) age 14-65 years old, inpatient or outpatient, male or female; (2) meet the diagnostic criteria of clinically diagnosed primary acral or sporadic in patients with acromegaly leukoplakia, or skin lesions symmetrically distributed in the sacral iliac carina parts; (3) subjects volunteered to participate, be required to sign an informed consent form; (4) whether or not the body with or without white spots, hands back or carina parts (such as sacral iliac sudden Long) needs with white markings and basic symmetrical on both sides at least there is a greater than 1cm; (5) All cases must for the progress of patients; (6) regardless of previous treatment.

Exclusion criteria

Exclusion criteria: (1) pregnant and lactating women; (2) serious heart, liver, renal insufficiency; (3) pre-cancerous skin lesions; (4) systemic lupus erythematosus (SLE), dermatomyositis ultraviolet treatment contraindications; (5) with immunosuppressive therapy; (6) hand infection or past treatment caused skin damage is not significant improvement or treatment; (7) secondary vitiligo (secondary to discoid lupus erythematosus, chronic eczema, vitiligo); (8) can not adhere to treatment.

Design outcomes

Primary

MeasureTime frame
Lesions chang;

Countries

China

Contacts

Public ContactXing-hua Gao
gaobarry@hotmail.com+86 13940152467

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 23, 2026