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临床试验/CTRI/2026/07/113626
CTRI/2026/07/113626进行中(未招募)不适用

Effectiveness of Topical Anthocyanin-Rich Blueberry Chitosan Nanoemulgel in management of Oral Leukoplakia: A Clinical Trial - BLUE-OL Trial

Saveetha Dental College and Hospitals0 个研究点入组 34 人开始时间: 2026年7月31日最近更新:
干预措施

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
34

研究概览

简要总结

暂无简介。

研究设计

研究类型
干预性

入排标准

入选标准

  • Oral leukoplakia Van der Waal Stage I and Stage II lesions.
  • Patients who have not undergone any previous treatment for oral leukoplakia.
  • Patients willing to provide written informed consent.
  • Patients willing to attend follow up visits at baseline, 15th day and 30th day.

排除标准

  • Oral leukoplakia Van der Waal Stage III and Stage IV lesions.
  • Patients with other oral potentially malignant disorders.
  • Patients with histopathological evidence of severe dysplasia or malignancy.
  • Pregnant and lactating women.
  • Patients allergic to anthocyanin, chitosan or tretinoin.
  • Patients with uncontrolled systemic disease or immunocompromised status.

研究组 & 干预措施

Intervention1: Anthocyanin Rich Blueberry Chitosan Nanoemulgel: Topical application of anthocyanin rich blueberry chitosan nanoemulgel over the oral leukoplakia lesion twice daily for 30 days

干预措施: Intervention1: Anthocyanin Rich Blueberry Chitosan Nanoemulgel: Topical application of anthocyanin rich blueberry chitosan nanoemulgel over the oral leukoplakia lesion twice daily for 30 days

研究者

标识符

CTRI 编号
CTRI/2026/07/113626

日期

首次发布
(2个月前)
最近更新
(上个月)

监管与共享

是否有结果
否