跳至主要内容
临床试验/NCT01856166
NCT01856166已完成不适用

Programmed Intermittent Epidural Bolus Coupled With PCEA (PIEB-PCEA) Versus Continuous Epidural Infusion Coupled With PCEA (CEI-PCEA) for Labor Analgesia in Nulliparous: Effects on Labor Outcomes

University Hospital, Montpellier4 个研究点 分布在 1 个国家目标入组 304 人开始时间: 2013年6月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
304
试验地点
4
主要终点
Occurence of a specific clinical criteria which can lead to a complication of the delivery

研究概览

简要总结

Epidural analgesia still have an impact on obstetric outcomes and especially on instrumented delivery rates.

To assess the best maintainance regimen of epidural analgesia during labor the investigators plan to include 300 nulliparous in this multicenter randomized, double blind trial. The primary outcome will be a composite set of criteria that can lead to instrumented delivery. Secondary outcome will focus on analgesia motor block and satisfaction.

详细描述

Patients will be informed during the anaesthetic consultation and recruited at the beginning of the labor if they comply with inclusion criteria. Habitual proceedings of the placing and induction of epidural analgesia (Local Anaesthetics (AL): Levobupivacaine 0.100% 15mL Sufentanil 10µg). Patients who will not obtain at 30min a pain score < 1/10 will be excluded (epidural analgesia not functional). The upkeep of analgesia will be provided by an automatic pump and randomized in: classic pump and new pump. The mixture used will be the same in the 2 groups: Levobupivacaine 0.0100% + Sufentanil 0.5µg/mL. The classic pump administers AL with a continuous output (8mL/h)even though the new pump administers AL in bolus (8mL every hour; beginning 1h after the induction). The classic pump is a pump CADD SMITHS PCEA (Patient Controlled Epidural Analgesia) with the programming: continuous output 8mL/h; Additional bolus if necessary: 8mL; Maximal dose by hour: 24mL.

The new pump is a pump CADD SMITHS called PIEB (Programmed Intermittent Epidural Bolus) with the programming: intermittent bolus 8mL every hour; Additional bolus if necessary: 8mL; Ban period during 10min between patient bolus and automatic bolus; Maximal dose by hour: 24mL.

In case of the pain reappears and which is not calmed with 2 successive patient bolus, the anaesthetist will be called for the evaluation and administration of a doctor bolus if necessary (Levobupivacaine 0.125% 5mL associated with 50µg of Clonidine).

Collected data will be demographic data, data about the obstetrical labor proceedings, data about pain, motor block, maternal satisfaction, total quantity of administered analgesia, number of patient and doctor bolus wich are asked and administered and neonatal data.

Endpoints will be collected by a doctor in blind of the type of pump (the 2 pumps are the same extern aspect, only the intern programming is different).

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Health Services Research
盲法
Triple (Participant, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 44 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • Nulliparous patient with a spontaneous labor at full term, from a normal pregnancy, carrier a singleton in cephalic position, with a distension <4cm and eligible for an epidural analgesia
  • Patient has signed informed consent
  • Patient affiliated or beneficiary of a social medical insurance
  • Patient aged between 18 and 44 years old

排除标准

  • Morphinic administration before the care
  • Anomaly of fetal cardiac rate
  • Fetal or maternal anomalies wich don't allow to evaluate motor block
  • Known uterine malformation
  • Contraindications for thrusts for pregnancy
  • Patient protected by law
  • Patient under guardianship

研究组 & 干预措施

CEI-PCEA

Active Comparator

Continuous Epidural Infusion coupled with Patient Controlled Epidural Analgesia

干预措施: Release analgesia by CADD SMITHS PCEA pump (Device)

CEI-PCEA

Active Comparator

Continuous Epidural Infusion coupled with Patient Controlled Epidural Analgesia

干预措施: Levobupivacaine (Drug)

CEI-PCEA

Active Comparator

Continuous Epidural Infusion coupled with Patient Controlled Epidural Analgesia

干预措施: Sufentanil (Drug)

PIEB-PCEA

Experimental

Programmed Intermittent Epidural Bolus coupled with Patient Controlled Epidural Analgesia

干预措施: Release analgesia by CADD SMITHS PIEB pump (Device)

PIEB-PCEA

Experimental

Programmed Intermittent Epidural Bolus coupled with Patient Controlled Epidural Analgesia

干预措施: Levobupivacaine (Drug)

PIEB-PCEA

Experimental

Programmed Intermittent Epidural Bolus coupled with Patient Controlled Epidural Analgesia

干预措施: Sufentanil (Drug)

结局指标

主要结局

Occurence of a specific clinical criteria which can lead to a complication of the delivery

时间窗: Up to 10 hours

Specific clinical criteria are: * Type of posterior engagement * Type of posterior extrication * Duration of waiting at complete dilatation \> 3 hours * Duration of expulsive efforts \> 40 minutes * Foetal bradycardia \< 100 BPM during 1 minute at least

次要结局

  • Instrumental delivery rate(up to 10 hours)
  • Pain during the end of labor(up to 10 hours)
  • Efficacity of epidural analgesia(up to 10 hours)
  • Presence of motor block(Up to 10 hours)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (4)

Loading locations...

相似试验