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临床试验/NCT02762773
NCT02762773终止不适用

Does Avoiding Inferior Rectus Sheath Dissection Lead to Decreased Operative Blood Loss and Operating Time Without Increasing Delivery of Fetus in Primary Cesarean Delivery

University Hospitals Cleveland Medical Center2 个研究点 分布在 1 个国家目标入组 81 人开始时间: 2018年2月1日最近更新:
适应症

试验速览

阶段
不适用
状态
终止
入组人数
81
试验地点
2
主要终点
post-operative hemoglobin

研究概览

简要总结

The purpose of this study is to evaluate the effect of non-dissecting the inferior rectus sheath during primary cesarean delivery on post-operative hemoglobin and post-operative pain control as measured by VAS score and opioid anesthesia use in the first 72 hours post-op.

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
Single (Participant)

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

  • - Patients must be 18 years or older as well as willing and able to provide informed consent
  • Patients undergoing a scheduled or non-scheduled, non-urgent or non-scheduled urgent (delivery within 30 minutes of decision for surgical delivery) Cesarean delivery between >35 weeks gestational age,
  • Patients who are expected to receive a Pfannenstiel incision
  • Patients with viable singleton intra-uterine pregnancy
  • Patients with fetus in cephalic presentation

排除标准

  • - Patients younger than 18 years,
  • Patients unable or unwilling to provide informed consent,
  • Patients who are illiterate,
  • Patients who are non-English speaking or reading,
  • Patients who are medical or nursing students at a school affiliated with University Hospital
  • Multi-fetal gestations (>1 intrauterine pregnancy),
  • Patients with a BMI >50 kg/m^2
  • Patients with a suspected placenta accreta or placenta previa
  • patients with 2 prior cesarean deliveries
  • Patient undergoing emergent cesarean delivery (delivery within 10 minutes of decision for surgical delivery)
  • Patients who will require a vertical skin incision, Maylard or Cherney incisions
  • Patients with a history of significant pelvic adhesive disease, as determined by prior operative reports
  • Patients with fetus in non-cephalic presentation
  • Patients with pre-gestational or gestational diabetes mellitus
  • Patients with estimated fetal weight >5000 grams
  • Patients with estimated fetal weight <10% for gestational age
  • Patients with who require general anesthetic
  • Patients who are on chronic pain medication
  • Patients with a history of drug abuse

结局指标

主要结局

post-operative hemoglobin

时间窗: 24 hours

assessment of drop in hemoglobin post-operatively compared to pre-operative values

次要结局

  • assessment of Visual Analog Scale (VAS) scores in first 72 hours(72 hours)
  • Assessment of total narcotic use, expressed as morphine equivalents(72 hours)

研究者

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

Emily Daggett

Principal Investigator

University Hospitals Cleveland Medical Center

研究点 (2)

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