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临床试验/CTRI/2012/04/002592
CTRI/2012/04/002592已完成3 期

A phase III randomized, double blind, multi-center study of Xylentraâ?¢ versus Silver Sulfadiazine forefficacy and safety in patients with partial thickness burns in India

Issar Pharmaceuticals Private Limited0 个研究点目标入组 200 人开始时间: 待定最近更新:

试验速览

阶段
3 期
状态
已完成
发起方
入组人数
200

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

  • Adult male or female patients aged 18- 60 years of age.
  • Patients with diagnosed (clinically) partial thickness thermal burn
  • Total surface area of the burn 10-20% by Wallace rule of Nine
  • (Appendix 8)
  • Willing to give written informed consent.
  • Females of child-bearing potential with a negative urine or serum
  • pregnancy test on admission and agrees to take suitable method of
  • contraception for the duration of the study
  • Weight range within 20% of the ideal body weight as per standard
  • tables and Indian criteria

排除标准

  • Patients with pulmonary burns
  • Patients with full thickness burns or deep partial thickness burn.
  • Patients who need skin grafting.
  • Patients with chemical or electrical burns.
  • Immune compromised patients. (patients taking
  • immunosuppressive drugs such as glucocorticoids, alkylating agents,
  • antimetabolites, antibodies, cyclosporin, tacrolimus, sirolimus,
  • interferons, opioids, TNF binding proteins, Mycophenolate or any
  • other biological agents)
  • Patients with history of chronic GI, renal, hepatic, respiratory,
  • infectious, or History of allergy or hypersensitivity to investigational
  • drugs or autoimmune disorders.
  • Any chronic condition requiring the use of systemic corticosteroids
  • 30 days prior to study entry and anytime during the course of the
  • Known or newly diagnosed diabetics requiring insulin or oral anti
  • Pregnant or breast-feeding female.
  • Known or suspected allergies to Xylentra• or silver sulfadiazine.
  • Participation in another investigational drug study within 30 days
  • prior to treatment start
  • Patients with history of any topical or systemic antimicrobial drug
  • for the current wound or taking antibiotics for co morbid condition
  • Patients suffering from any medical illnesses after burn which
  • investigator thinks will endanger patientâ??s condition.

研究者

发起方
Issar Pharmaceuticals Private Limited

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