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临床试验/CTRI/2018/03/012591
CTRI/2018/03/012591招募中未知

To study the efficacy and safety of intra-operative use of Platelet rich plasma(PRP) in autologous non cultured epidermal cell suspension (NCECS) grafting when compared to autologous non cultured epidermal cell suspension alone in surgical management of stable vitiligo. - NCS-PRP

Intitutional research committee0 个研究点目标入组 0 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
招募中
发起方

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

入选标准

  • Patients with stable Vitilgo with no increase in size of lesion for past 06 months

排除标准

  • 1) Unstable vitiligo (New lesion or extension of pre-existing lesion)
  • 2) Vitiligo stabilized on systemic medical therapy
  • 3) Evidence or history of keloid/hypertrophic scars.
  • 4) Patients with chronic auto immune and infectious diseases e.g. DM, Thyroid disease, HTN, Hep B,C,HIV etc.
  • 5) Patients with bleeding disorders or on medications affecting platelet function e.g. Ecosprin.

研究者

发起方
Intitutional research committee

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