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临床试验/NCT02055794
NCT02055794已完成不适用

Promoting Optimal Healing After Laceration Repair Study - PALS Study

University of Michigan2 个研究点 分布在 1 个国家目标入组 35 人开始时间: 2014年2月最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
35
试验地点
2
主要终点
Patient-perceived pain

研究概览

简要总结

The goal of this research is to investigate three different methods of perineal skin closure during second-degree perineal wound repair and determine which method is associated with the least amount of patient pain.

Null hypothesis: There will be no difference in patient pain among the three different methods for second degree perineal wound repair.

详细描述

At the University of Michigan, there are currently two standard techniques for repairing second-degree perineal lacerations that differ only in management of the perineal skin :

  1. Closure of the deep tissues and superficial perineal skin using a continuous 3-0 Vicryl suture
  2. Closure of the deep tissues with a continuous 3-0 Vicryl suture and reapproximation of, but not suture-closure of the perineal skin.

The primary goal of our study is to compare patient pain amongst the following three perineal skin repair techniques after second degree laceration:

  1. Perineal skin closure with suturing
  2. Not suturing the perineal skin
  3. Closure of the perineal skin with n-Butyl 2-cyanoacrylate (Indermil®) surgical glue.

In all women, the deep vaginal and perineal tissues will be closed using a continuous 3-0 Vicryl suture, as is current standard practice.

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
Double (Participant, Investigator)

入排标准

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

入选标准

  • Women 18 years old - 45 years old
  • Immediately post-vaginal birth, including forceps-assisted vaginal delivery, vacuum-assisted vaginal delivery
  • > 32 weeks gestation
  • Second degree laceration from spontaneous tear or midline episiotomy
  • Proficient in English

排除标准

  • <18 years old and >45 years old
  • Delivery by Cesarean
  • 1st, 3rd or 4th degree lacerations
  • Induction for intrauterine fetal demise or terminal fetal condition, or any instance where immediate status of the newborn is unknown
  • Known allergy to cyanoacrylate or formaldehyde
  • Systemic infections, uncontrolled diabetes (women with well-controlled pre-gestational or gestational diabetes will not be excluded)
  • History of connective tissue disorders (e.g. Scleroderma, Ehlers Danlos)
  • Chronic use of steroids
  • Currently under treatment for cancer
  • Previous radiation to the pelvis
  • Any organ transplants
  • History of neurological conditions including multiple sclerosis, stroke, Alzheimer's, or other dementias
  • Not proficient in the English language

研究组 & 干预措施

Suturing of the perineal skin

Active Comparator

Suturing of the perineal skin after deep vaginal and perineal tissues are closed using a continuous 3-0 Vicryl suture.

干预措施: Suturing of the perineal skin (Procedure)

No suturing of the perineal skin

Active Comparator

No suturing of the perineal skin after deep vaginal and perineal tissues are closed using a continuous 3-0 Vicryl suture.

干预措施: No suturing of the perineal skin (Procedure)

Closing perineal skin with surgical glue

Active Comparator

Closure of the perineal skin with n-Butyl 2-cyanoacrylate (Indermil®) surgical glue after deep vaginal and perineal tissues are closed using a continuous 3-0 Vicryl suture.

干预措施: Closing perineal skin with surgical glue (Procedure)

结局指标

主要结局

Patient-perceived pain

时间窗: Post-partum (PPD), 2 weeks, 6 weeks and 3 months.

The 2 week and 3 month measurements will be done via email, web or mailed questionnaire. Pain will be measured using 3 pain scales: a validated 100-mm Visual Analogue Scale (VAS) (anchors: 0 = none, 100 mm = worst imaginable), a 6 point Likert scale and the McGill pain questionnaire short form.

次要结局

  • Wound assessment(6 weeks post-partum)

研究者

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

Dee Fenner

Professor, Obstetrics & Gynecology

University of Michigan

研究点 (2)

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