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临床试验/CTRI/2025/12/098374
CTRI/2025/12/098374尚未招募2/3 期

A Randomized Controlled Clinical Trial to Evaluate the Efficacy of Dhatturadi Taila as compared to the efficacy of Vipadikahar Ghrita Taila in Vipadika.

All India Institute of Ayurveda Dhargal Goa1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2026年1月15日最近更新:

试验速览

阶段
2/3 期
状态
尚未招募
发起方
入组人数
60
试验地点
1

研究概览

简要总结

Current management strategies for palmoplantar psoriasis involve topical treatments (corticosteroids), Phototherapy

  • Psoralen And Ultraviolet A (PUVA), systemic immunomodulators (Ciclosporin, Azathioprine, Methotrexate, etc), and biologic agents (Infliximab, Ustekinumab, etc), however, these approaches often come with limitations like a relapse of the skin lesions after discontinuing the treatment, the potential to create skin cancer, melanomas, high cost, and potential immunosuppressive side effects.

Acharya Sushruta has mentioned Kushta as one of the complications of Dooshivisha. Hence, an effort is needed to look for Dooshivisha hetu among patients with Kushta with special reference to Vipadika.

Hence, this is an effort to evaluate the efficacy of the external application of Dhatturadi Taila for chronic skin conditions such as Vipadika in a Controlled Clinical Trial along with Dooshivisha hetu among the patients with vipadika.

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
None

入排标准

年龄范围
18.00 Year(s) 至 60.00 Year(s)(—)

入选标准

  • Clinically diagnosed patients with Vipadika as per WHO TM2 SN9Y.
  • Patients of the 18 to 60 years of age group of any Gender, Religion, socio-economic status, or Geographical area.
  • Mild to Moderate cases of Vipadika having any 2 cardinal symptoms of Vipadika ie Panipadasphutanam, manda kandu, tivra Vedana, rukshata 4)Patients with m-PPPASI less than or equal to 50 5)Patients with DLQI less than or equal to 21 6)Patients with NRS less than or equal to 7 7)Participants who have discontinued allopathic treatment at least two weeks before.
  • (Washout Period More than or Equal to 2 weeks) 8)Symptoms for at least 3 months 9)Able to comply with all study procedures for the duration of the study.

排除标准

  • Patients already diagnosed with Uncontrolled Diabetes 2)Children, Pregnant and Lactating Women 3)Immunocompromised patients (e.g. HIV infection, Hepatitis) 4)Patients having other associated skin disorders 5)Patients who have sensitivity reactions to the medicated oils 6)Vipadika skin disease with secondary infections.

研究者

发起方
All India Institute of Ayurveda Dhargal Goa
申办方类型
Other [MD Dissertation ]
责任方
Principal Investigator
主要研究者

ADITYA YUVRAJ HATWAR

All India Institute of Ayurveda, Goa

研究点 (1)

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