CTRI/2020/08/027070尚未招募未知
A Prospective, Single-center, Open label, Randomized, Parallel-group, Active-controlled Clinical Study to Evaluate the Efficacy and Safety of FDC of Trypsin plus Bromelain plus Rutoside trihydrate given along with Cefuroxime axetil versus Cefuroxime axetil for Healing in Patients with Surgical Wound after Minor Surgery
okmanya Medical Research Center0 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
- 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. Adult male or female patients aged between 18 to 65 years of age
- •(both ages inclusive)
- •2. Diagnosed with surgical wounds after minor surgery mainly
- •REF/2020/06/034654
- •CTRI Website URL - http://ctri.nic.in
- •involving skin and skin
- •structure infections
- •3. Women of childbearing potential must be willing to consistently
- •use an appropriate
- •method of contraception
- •4. Willingness to give their written informed consent to participate in
- •5. Is willing to comply with all aspects of the protocol
排除标准
- •1. Patients with known hypersensitivity to active ingredients or
- •inactive ingredients of the
- •study treatment or other ?-lactams (e.g., penicillins and
- •cephalosporins) except study
- •2. Female patients who are pregnant or lactating or planning to be
- •3. Patients with known history of clostridium difficile-associated
- •4. Patients receiving medicines such as tetracycline group of drugs,
- •amoxicillin, aspirin, and
- •anticoagulants including clopidogrel.
- •5. Currently receiving treatment with IP or systemic or topical
- •antibiotics or systemic
- •therapy with cytotoxic drugs.
研究者
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