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临床试验/NCT04621994
NCT04621994Unknown不适用

Cesarean Wound Closure: Dermabond Versus Steri Strips

University of Tennessee0 个研究点目标入组 133 人开始时间: 2020年11月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
入组人数
133
主要终点
Patient and Observer Scar Assessment Scale Surveys (POSAS)

研究概览

简要总结

The purpose of this study is to determine overall patient satisfaction with their cesarean section scar with application of Steri-strips vs. Dermabond following subcuticular skin closure of pfannenstiel incision

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 45 Years(Adult)
性别
Female
接受健康志愿者
是

入选标准

  • •Women age 18-45 who are undergoing planned or unscheduled cesarean section at Regional One Health
  • •Gestational age > 24 weeks
  • •Planned Pfannenstiel incision
  • •Willing to consent to the study

排除标准

  • •Emergency or urgent cesarean section
  • •Vertical skin incision
  • •Intrapartum intraamniotic infection
  • •Unwilling to consent to the study

研究组 & 干预措施

Steri Strips Arm

Active Comparator

干预措施: Steri Strips (Other)

Dermabond Arm

Experimental

干预措施: Dermabond (Other)

结局指标

主要结局

Patient and Observer Scar Assessment Scale Surveys (POSAS)

时间窗: at 1 weeks postpartum

Validated scale comparing a scar to normal skin. Score ranges from 6 to 60 with the higher numbers less like normal skin.

Patient and Observer Scar Assessment Scale Surveys

时间窗: at 6 weeks postpartum

Validated scale comparing a scar to normal skin. Score ranges from 6 to 60 with the higher numbers less like normal skin.

次要结局

  • Number of patients with wound separation or dehiscence(through 6 weeks postpartum)
  • Number of patients with wound infection(through 6 weeks postpartum)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Laura Grese Willingham

Assistant Professor

University of Tennessee

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