RPCEC00000046已完成3 期
se of tissue adhesive Tisuacryl® in the closure of skin wounds
Center of Biomaterials of Havana University0 个研究点目标入组 674 人开始时间: 2008年9月30日最近更新:
适应症
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 发起方
- 入组人数
- 674
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
- N/a: Single Arm Study. Masking: Open. Control Group: Uncontrolled. Assignment: Single Group. Purpose: Treatment
入排标准
- 年龄范围
- 1 years 至 80 years（—）
- 性别
- All
入选标准
- •Patients of both genders, between 1 and 80 years old. Adult patients who gave the informed consent. Children whose parents or tutors signed the informed consent. Patients who fulfill the established diagnostic criteria:: 1)Surgical incisions less than 6 cm long which had subcutaneous sutures. Longer incisions could be considered using anchor sutures every 3-4 cm. 2)Recent (under 6 hours) non deep cutaneous lacerations (that do not require internal suture) less than 4 cm long and 0.5 cm in width.
排除标准
- •Patients with wounds contaminated by any foreign body Patients with wounds produced by bites or scratch of animals or humans, puncture or crushing Patients with wounds located in an area of high skin tension Patients with mental incapacity and/or severe psychological disorders Pregnant and breastfeeding women Patients that do not consent to participate in the study
研究者
相似试验
已完成
3 期
Tisuacryl® in DentistryOral and facial surgical incisions and traumatic lacerationsFacial InjuriesWounds and InjuriesMouthFaceRPCEC00000044Center of Biomaterials of Havana University439
已完成
2 期
Tisuacryl® in esophageal surgeryEsophageal StenosisEsophageal cancer or benign stenosisEsophageal NeoplasmsGastrointestinal NeoplasmsDigestive System NeoplasmsEsophageal DiseasesGastrointestinal DiseasesDigestive System DiseasesRPCEC00000045Center of Biomaterials of Havana University58
尚未招募
2 期
Comparison of silk suture and cyanoacrylate adhesive after mandibular third molar surgical removalCTRI/2021/01/030720usrin Thoniyotupurayil
尚未招募
不适用
Comparison of clinical efficacy and esthetic outcomes between n-butyl cyanoacrylate tissue adhesive and prolene suture material for wound closure in orbital floor and orbital rim fracture fixatioCTRI/2021/03/031927Dr Asha V Shet
已完成
不适用
Central venous Access device SeCurement And Dressing Effectiveness: the CASCADE TrialCentral venous access device failure prior to completion of therapyPublic Health - Health service researchACTRN12613001103752Griffith University2,444