Hydrocolloid Dressings for Oculofacial Plastic and Reconstructive Wound Healing
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 10
- 试验地点
- 3
- 主要终点
- Number of participants with wound dehiscence
研究概览
简要总结
This study aims to explore the use of a hydrocolloid dressing (DuoDERM EXTRA THIN) as an alternative to the current standard of care. The dressing would be applied immediately after surgery and removed at a post-operative week 1 appointment. The dressing would eliminate the need for antibiotic ointment application and reduce the burden of post-operative care on the patient.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Supportive Care
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 100 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Patients >18 years of age
- •follow-up at specified intervals (1 week/6 week/3 months) in an office setting
- •can give informed consent
- •no patients will be excluded on the basis of gender, ethnicity, or religious background
排除标准
- •Patients <18 years of age or >100
- •allergy to pectin, gelatin, and sodium carboxymethylcellulose
- •adults with impaired consent capacity
- •incarcerated individuals.
研究组 & 干预措施
Wound Dressing
At the conclusion of the surgical procedure, patients will receive topical wound dressing to surgical sutured periocular wounds
干预措施: Hydrocolloid Wound Dressing (Device)
Antibiotic Ointment (Control)
At the conclusion of the surgical procedure, patients will receive topical antibiotic ophthalmic ointment to surgical sutured periocular wounds
结局指标
主要结局
Number of participants with wound dehiscence
时间窗: 3 months
YES/NO type question if wound dehiscence is present after removal of the patch
次要结局
- Patient and Observer Scar Assessment Scale(3 months)
研究者
Janice Hernandez, MD
Instructor
University of Kentucky