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临床试验/CTRI/2023/03/051181
CTRI/2023/03/051181尚未招募Unknown

Study of efficacy and safety of oral tofacitinib vs azathioprine in the management of chronic actinic dermatitis-An open randomised clinical trial

Krishna Vishwa Vidyapeeth0 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
Unknown
状态
尚未招募
发起方

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

入选标准

  • 1. Patients with Clinical diagnosis of chronic actinic dermatitis including:
  • Actinic Prurigo
  • Actinic cheilitis
  • Lichenoid photodermatitis
  • Photoallergic dermatitis
  • Phytophotodermatitis
  • Actinic reticuloid
  • 2. Age group more than 18 years of age.
  • 3. The patient should have given written consent before the investigations and starting the drug.
  • 4. The patient should be able and willing and fit, in the view of the investigator, to comply with all study procedures

排除标准

  • A .Patients with acute photodermatitis.
  • B. Patients allergic to tofacitinib or azathioprine.
  • C. Patient with cardiac diseases or hematological diseases (including angina, coronary artery disease, recent or acute myocardial infarction, pericardial effusion,anemia,coagulation disorders)
  • D. Patients with cerebrovascular diseases
  • E.Patients with deranged liver and kidney function.
  • F. Patients with recent infections.
  • G. Patient with positive mantoux test.
  • H.Patients with a recent or past history of tuberculosis
  • I.Patient with a positive Interferon Gamma Release Assay (IGRA) test.
  • J.Patients with a history of acute phototoxic diseases.
  • K.Phototoxic rash related to some drug.
  • L.Patients with Low Thiopurine Methyl Transferase(TPMT) value ( < 0.5 U). M.Pregnant,lactating or women of child bearing age group with incomplete family. N.Patients with positive HIV,HCV or HbsAg.
  • O.Patients having diabetes mellitus.
  • P.Patients with any immunocompromised conditions.

研究者

发起方
Krishna Vishwa Vidyapeeth

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