CTRI/2021/03/031887
尚未招募
3 期
Evaluate the efficacy of topical autologous platelet rich plasma in treatment of moderate- severe dry eye.
概览
- 阶段
- 3 期
- 干预措施
- 未指定
- 疾病 / 适应症
- 未指定
- 发起方
- Department of ophthalmology
- 状态
- 尚未招募
- 最后更新
- 4年前
概览
简要总结
暂无简介。
研究者
入排标准
入选标准
- •1\.Schirmerâ??s \<\=10 mm in 5 min
- •2\.TBUT \<\=10 seconds
- •3\.Age range: 18 years \- 90 years.
- •4\.Able to acknowledge and give informed written consent.
- •5\.Able to co\-operate with the investigational plan and obey all mandatory follow\-up visits.
排除标准
- •1\.Patients who are unwilling or unable to give consent, refuse to accept randomization, or to return for scheduled visits.
- •2\.Involved in other clinical trial.
- •3\.Uncooperative patients.
- •4\.Patients under 18 or more than 90 years age.
- •5\.Pregnant females or expecting to become pregnant during the study.
- •6\.AIDS or other systemic immune deficient conditions or are under systemic immunosuppressants.
- •7\.Contact lens wear
- •8\.Active ocular infection
- •9\.Unable to close eyes or uncontrolled blinking
结局指标
主要结局
未指定
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