ACTRN12613000182796已完成未知
Feasibility Study Assessing 14 days of Postoperative Pain after a single direct application of an Oral Wound Dressing in Post-Tonsillectomy Adults
Medtronic Australasia Pty Ltd.0 个研究点目标入组 36 人开始时间: 2013年2月15日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 36
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomised controlled trial
- 主要目的
- Treatment
- 盲法
- Blinded (masking used)
入排标准
- 年龄范围
- 18 Years 至 50 Years（—）
- 性别
- All
入选标准
- •18 – 50 years of age
- •Indicated for tonsillectomy due to obstructive breathing tonsil hyperplasia, tonsillitis or other chronic throat-related illness
排除标准
- •Prior tonsillectomy or tonsillotomy
- •Concurrent surgical procedures (including adenoidectomy)
- •Subject has a known shellfish allergy
- •Body Mass Index (BMI) greater than 35
- •Known bleeding disorder or prescribed anticoagulants
- •Cranial facial abnormalities that may interfere with access to the tonsils
- •Subject is immunocompromised (e.g., taking immunosuppressive medication)
- •Chronic or frequent use of pain medications
- •Subject has a serious comorbid condition that may interfere with the conduct or results of the clinical study
- •Subject is currently participating in another clinical study and has not been approved for concurrent enrolment by the Study Sponsor.
- •Subject is pregnant or breast-feeding
研究者
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