CTRI/2010/091/000279已完成3 期
A Comparative, Randomized, Double blind, Multicentric, Clinical Study to Evaluate the Efficacy, Safety and Tolerability of Besifloxacin ophthalmic suspension 0.6% Vs Moxifloxacin ophthalmic solution 0.5% in patients with Bacterial conjunctivitis.
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 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
- •1. Must have a diagnosis of acute bacterial conjunctivitis and exhibit purulent conjunctival discharge and redness in at least one eye.
- •2. Patients providing written informed consent to participate in the trial.
排除标准
- •1. Patients < 18 & > 60 years.
- •2. Pregnant or nursing females
- •3. Known hypersensitivity to fluroquinolones or to any of the study ingredients.
- •4. Use of any antibiotic within 72 hours of treatment.
- •5. Any disease or condition that could interfere with the safety and efficacy evaluations of the study medications.
- •6. Participation in an ophthalmic drug or device research study within 30 days prior to entry into the study.
研究者
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