CTRI/2018/05/013756已完成4 期
A comparative study of the efficacy and tolerability of Co-amoxiclav, Cefpodoxime Proxetil and Levofloxacin in acute, uncomplicated bacterial tonsillitis.
试验速览
- 阶段
- 4 期
- 状态
- 已完成
- 入组人数
- 90
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
- •Subjects of either gender between 10 - 55 years diagnosed as acute bacterial tonsillitis as confirmed by throat swab.
- •Willingness to give written informed consent and availability for regular scheduled follow up.
排除标准
- •Subjects with suspected viral tonsillitis.
- •Subjects with complications like quinsy, parapharyngeal abscess, AOM, suppurative cervical adenitis.
- •Subjects with coexisting LRTIs / sinusitis
- •Patients with severe renal and/or hepatic dysfunction
- •Pregnant and lactating women
- •Those who had taken antibiotics within the previous 48 hours or those who had received long acting penicillins within 2 weeks before enrolment into the study.
- •Subjects with history of any hypersensitivity/or any SAE, to any of the study medications.
- •Immunocompromised subjects, and in the presence of disorders associated with muscle weakness.
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