Evaluation of Safety and Efficacy of Using Seraffix LTB - (Laser Tissue Bonding) System
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 15
- 试验地点
- 1
- 主要终点
- Primary study endpoint will be to establish the safety of using the Seraffix System for tissue bonding and wounds closure. Safety will be established by paucity of serious adverse events and adverse events.
研究概览
简要总结
The purpose of this study is to evaluate the safety and effectiveness of using Seraffix LTB system for soft tissue bonding.
详细描述
Dermatologic wounds can be closed by a variety of methods. The choice of a particular closure technique should be based on the patient, wound, tissue characteristics, and anatomic location. The purpose of these closure methods is an approximation of wound lips until the regenerate tissue reach a phase, where it is closed and can sustain the daily tensile forces.
Several methods are used for wounds closure such as sutures, staples, tapes, tissue adhesives and laser energy. There have been two fundamental approaches to laser assisted bonding of tissues:
- Laser welding-heating the approximated edges of cuts in tissues by a laser beam;
- Laser soldering- applying a biological solder onto the approximated edges and heating the solder (and the underlying tissue).
Seraffix has developed the Seraffix LTB (Laser Tissue Bonding) System - a laser system for soft tissue bonding. This innovative system includes features that make laser soldering suitable for clinical use. The Seraffix system is composed of CO2 laser device, propriety grip device (Clamps) and soldering agent (Human Albumin).
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 60 Years（Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Male/Female age 18-
- •Subject is scheduled for laparoscopic cholecystectomy surgery.
- •Subject able to comprehend and give informed consent for participation in this study.
- •Signed informed consent form.
排除标准
- •Unstable angina and/or congestive heart failure requiring hospitalization within the last 6 months prior to screening.
- •Acute infection requiring intravenous antibiotics at the time of screening.
- •Bleeding, coagulation and or clotting disorders.
- •Diabetes mellitus: IDDM or NIDDM.
- •HIV positive or any other immunosuppressive disorder.
- •Renal failure (Serum creatinine >2.0 mg/dl).
- •Inflammatory and or allergic diseases or condition of the skin: Psoriasis, Eczema or dermatitis.
- •Any concomitant infection - viral or bacterial.
- •Drug abuse.
- •Use of steroids.
- •Infection / abscess / pain in treatment target area.
- •Pregnancy or lactating.
- •History of keloid scarring.
- •Use of aspirin or antioxidants
- •Subject is suffering extreme general weakness.
- •Subject objects to the study protocol.
- •Known cognitive or psychiatric disorder
- •Concurrent participation in any other clinical study.
- •Physician objection.
研究组 & 干预措施
A
干预措施: Seraffix LTB (Device)
结局指标
主要结局
Primary study endpoint will be to establish the safety of using the Seraffix System for tissue bonding and wounds closure. Safety will be established by paucity of serious adverse events and adverse events.
时间窗: 3 months
次要结局
- 1. Re-intervention: A subject is scored a success (1) if he had No Re-intervention by 3 months; otherwise he is scored a failure (0). 2. Wound dehiscence of at least 50% of wound length:(3 months)