EUCTR2008-006903-22-NL进行中（未招募）不适用
arrow band UV-B phototherapy and fluticasone proprionate versus narrow band UV-B phototherapy and placebo for the treatment of active vitiligo: a randomized double blind controlled trial - UVBVIT
Academic Medical Center0 个研究点开始时间: 2008年12月9日最近更新:
适应症
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 进行中（未招募）
- 发起方
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
- 性别
- All
入选标准
- •i.Patients with active vitiligo, eligible for NB-UVB phototherapy;
- •ii.Subjects attending the outpatient department of the SNIP;
- •iii.Adult patients: = 18 years;
- •iv.Subject is willing and able to give written informed consent.
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range
- •F.1.3 Elderly (>=65 years) no
- •F.1.3.1 Number of subjects for this age range
排除标准
- •v.With a personal or a family history of skin cancer (non-melanoma skin cancer: first degree family members, melanoma: any family member)
- •vi.With a personal history of photosensitivity and/or phototoxicity disorders
- •vii.With skin type I (according to Fitzpatrick classification I-VI)
- •viii.Who are pregnant
- •ix.Who are taking medications known to cause photosensitivity and/or phototoxicity and chronic or very frequent use of any medication that can influence the UVB response (eg. tetracycline, retinoids, sulfonamids, psoralens, NSAID’s)
- •x.With other skin diseases that would impair evaluation of repigmentation, such as psoriasis and eczema.
- •xi. Who are not able to have 2 times weekly NB-UVB phototherapy
- •xii. With local immunosuppressive treatment or 6 weeks prior to enrolment. For these patients a washout period of 6 weeks will be required.
研究者
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