An observational study to assess utility of dermoscopy as a clinical response predictor in non-segmental vitiligo treated with narrow band ultraviolet B phototherapy, SMS medical college, Jaipur
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 发起方
- 入组人数
- 50
- 试验地点
- 1
- 主要终点
- Change in Vitiligo Area Scoring Index (VASI) after NB-UVB phototherapy, and correlation of dermoscopic findings with this change in patients with non-segmental vitiligo.
研究概览
简要总结
Vitiligo is a common skin disorder characterized by loss of pigmentation, which can significantly affect the quality of life of patients. Narrow band ultraviolet B (NB-UVB) phototherapy is a standard and widely used treatment for non-segmental vitiligo. However, the degree of clinical improvement varies among patients, and there is a need to identify early predictors of response to guide management.
Dermoscopy is a non-invasive tool that allows detailed visualization of skin structures not visible to the naked eye. Certain dermoscopic features may provide valuable information about disease activity and potential for repigmentation.
The present study is a prospective observational study being conducted in the Department of Dermatology, SMS Medical College, Jaipur. Patients with non-segmental vitiligo who are scheduled to undergo NB-UVB phototherapy and meet inclusion criteria will be enrolled after providing informed consent. Baseline dermoscopic findings of selected vitiligo patches (acral and non-acral sites whenever feasible) will be recorded. Patients will then undergo NB-UVB phototherapy for 12 weeks. Changes in vitiligo lesions will be assessed clinically using the Vitiligo Area Scoring Index (VASI), and correlated with baseline dermoscopic findings to evaluate their predictive value.
The primary outcome is to determine whether specific dermoscopic features can serve as predictors of clinical improvement in vitiligo patients receiving NB-UVB therapy. This may help in better counseling, early identification of likely responders, and optimizing treatment decisions in vitiligo management.
研究设计
- 研究类型
- Observational
入排标准
- 年龄范围
- 12.00 Year(s) 至 60.00 Year(s)(—)
- 性别
- All
入选标准
- •Patients with clinically diagnosed non-segmental vitiligo.
- •Presence of at least 3 vitiligo patches scheduled for NB-UVB phototherapy.
- •One acral (hands/feet/bony prominence) and one non-acral lesion will be selected whenever feasible.
- •Patient provides written informed consent.
排除标准
- •Patients who used systemic or topical medications for vitiligo in the past 4 weeks or receiving surgical treatment.
- •Patients with other significant dermatoses.
- •Pregnant or breastfeeding women.
- •Patients with history of photosensitizing disorders, sensitivity to phototherapy, or claustrophobia.
- •Uncooperative or unwilling participants.
结局指标
主要结局
Change in Vitiligo Area Scoring Index (VASI) after NB-UVB phototherapy, and correlation of dermoscopic findings with this change in patients with non-segmental vitiligo.
时间窗: Baseline (before starting NB-UVB) | 4 weeks of treatment | 8 weeks of treatment | 12 weeks of treatment
次要结局
- 1)Correlation of specific dermoscopic patterns (e.g., perifollicular repigmentation, pigment network) with extent of clinical improvement.
研究者
ANSHRUTA TEOTIA
Sawai Man Singh Medical College and hospitals
