跳至主要内容
临床试验/NCT04797637
NCT04797637已完成不适用

Post-operative Patient Positioning Device for Improvement of Post-Operative Pain in Parturients Undergoing Cesarean Delivery: A Randomized Controlled Trial

Vanderbilt University Medical Center2 个研究点 分布在 1 个国家目标入组 278 人开始时间: 2021年4月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
278
试验地点
2
主要终点
Total Morphine Milliequivalent (MME) Use Postoperatively After Cesarean Delivery

研究概览

简要总结

This paucity of evidence supporting or dissuading the use of postoperative abdominal support following cesarean section for the reduction of postoperative pain leaves important clinical questions unanswered. Additionally, there is an absence of long-term outcomes associated with the use of abdominal support devices. There remains a need for the development and implementation of nonpharmacologic methods for analgesia for women following cesarean sections, along with evidence-based recommendations regarding their use in postoperative patients. The ABBy (G-Squared Medical, Brentwood, TN) is an extended-wear panniculus retractor/tissue stabilizer that is intended for use postoperatively after abdominal procedure.

It is placed directly onto patient skin, superior to a transverse incision, and is then used to elevate redundant tissues away from an incision or wound (https://www.gsquaredmedical.com/How-it-Works.html). The ABBy can be removed and replaced by patients and can be used for up to 10 days. This study aims to assess the effect of ABBy use on postoperative pain, pain medication requirement, and patient satisfaction, when used as a patient-positioning device in women following cesarean delivery.

详细描述

BACKGROUND:

Postoperative pain has significant short- and long-term implications for parturients undergoing cesarean delivery. Poorly controlled postoperative pain can interfere with the women's ability to care for herself and her newborn in the immediate postoperative period, and can contribute to longer length of hospitalizations. Untreated pain is associated with persistent pain, postpartum depression, and greater opioid use.

It is well established that an individualized, multimodal analgesic plan for the management of postoperative pain following cesarean delivery is associated with superior pain relief and decreased opioid consumption. While different institutional guidelines influence general practice patterns, a combination of several medications acting on different receptors has been shown to be effective in decreasing postoperative pain. In 2018, the cesarean section rate in the United States was 31.9%, compared to 20.7% in 1996. As the cesarean delivery rate increases, it is becoming more pertinent to develop and incorporate nonpharmacologic practices for postoperative pain.

The use of abdominal binders as an adjunct to pharmacologic therapy for the management of postoperative pain following major abdominal surgery has previously been discussed in surgical literature.

The utility of abdominal support within the Obstetrics literature is both sparse and conflicting.

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 —(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • Age > 18 years
  • Cesarean delivery
  • <36 hours post-delivery

排除标准

  • Vertical skin incision
  • Inability to place device superior to incision
  • Presence of surgical drain
  • Opioid use disorder
  • Chronic opioid use (> 14 consecutive days during pregnancy)
  • Allergy to device adhesive
  • Active COVID-19 infection
  • Patient unable to consent

结局指标

主要结局

Total Morphine Milliequivalent (MME) Use Postoperatively After Cesarean Delivery

时间窗: 14 days postoperative

Postoperative analgesia will be administered to all participants as per routine guidelines on postpartum.

次要结局

  • Duration of Use of Patient Positioning Device.(Baseline to 14 days postoperative)
  • Surgical Costs in Groups With and Without Patient Positioning Device(Baseline to 14 days)
  • Subjective Pain Scores During Use of Patient Positioning Device(Baseline to 14 days postoperative)
  • Patient Satisfaction During Use of Patient Positioning Device.(Baseline to 14 days postoperative)
  • Number of Participants With Surgical Complications in Groups With and Without Patient Positioning Device(Baseline to 14 days)

研究者

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

Lisa C. Zuckerwise, MD

Assistant Professor of Obstetrics and Gynecology

Vanderbilt University Medical Center

研究点 (2)

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