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临床试验/NCT00727935
NCT00727935已完成4 期

Comparison Of The Analgesia Obtained By Infiltration Of Lidocaïne 1% And Ropivacaïne 0,75% Versus Placebo For The Joinings Of Episiotomies Among Parturients Under Epidural Analgesia

University Hospital, Angers2 个研究点 分布在 1 个国家目标入组 165 人开始时间: 2006年10月1日最近更新:
适应症
相关药物

试验速览

阶段
4 期
状态
已完成
发起方
入组人数
165
试验地点
2
主要终点
Time between the infiltration of the local anaesthetic and the first analgesics catch per os, which is managed when the level of pain evaluated by EVA is higher than 30 mm

研究概览

简要总结

Lateral episiotomy is a current care practiced with childbirth room. One of the problems encountered with this surgical act is the residual pain on perineal scar level. Maximal during the first 24 hours, this pain can persist several days or several weeks hampering to variable degrees a normal recovery of autonomy and comfort of life. Some studies have shown the interest of ropivacaine, local anaesthetic with a long action's duration for proctologic surgeries and for the cure of inguinal hernia. A recent study shown the ropivacaine perineal infiltration used prior perineorrhaphy allows an absence of post-partum pain for 24 to 27% of cases and a first analgesics request delayed to ten hours.

Methodology: 165 parturients having an epidural analgesia and an episiotomy were enrolled. The perineal infiltration was randomized according to 3 equal groups (placebo, ropivacaine 0,75%, lidocaine 1%) and realised prior perineorrhaphy. then The parturient were followed during the 24 first hours. This study was designed as double blind and the study conduct was standardized in order to get only variable such as the episiotomy infiltration.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Double

入排标准

年龄范围
18 Years 至 50 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • Pre-inclusion criteria :
  • Assent of participation in the study signed
  • Major parturient (> 18 years) in the course of work in room of childbirth
  • Mono-foetal pregnancy
  • Presentation at the top
  • Inclusion Criteria:
  • Checking of the criteria of pre-inclusion
  • Oral confirmation of the assent of the patient
  • ASA 1 or 2
  • Childbirth by low way
  • Patient having an epidural analgesia
  • Patient having an episiotomy
  • Counter-indication with the ropivacaïne

排除标准

  • Absence of signed assent of participation in the study
  • Counter indication with the lidocaïne
  • General counter-indications suitable for the epidural anaesthesia , independently of the local anaesthetic used
  • Counter-indications with the infiltration: patient under anticoagulants, coagulopathy
  • Allergy to the lidocaine or the ropivacaine
  • Allergy to the one of analgesics per bones used in the assumption of responsibility of routine
  • Severe insufficiency hepatic and/or renal and/or ulcerates gastro-duodénal (in the case of anti-inflammatory drug regulation not steroid during the postpartum)
  • Major protected within the meaning of the law Huriet
  • Patient during one time of exclusion following another biomedical study
  • Exclusion Criteria:
  • Absence of oral confirmation of the assent of the patient
  • Infection or ignition of the point of puncture
  • Analgesia epidural not functional
  • Dural breach
  • Appearance of ascribable side effects to only the anaesthetic buildings at the time of epidural analgesia
  • Median Episiotomy (increased risk of lesions of the sphincter)
  • Need for an instrumentation at the time of expulsion
  • Haemorrhage of the delivery requiring a blood transfusion and/or general anaesthesia in urgency with surgical operation for haemostasis

结局指标

主要结局

Time between the infiltration of the local anaesthetic and the first analgesics catch per os, which is managed when the level of pain evaluated by EVA is higher than 30 mm

时间窗: 1 year

次要结局

  • To compare between the 3 groups the mean level of the pain during the first 24 hours following the joining of the episiotomy, measured by EVA(24 hours)
  • To compare between the 3 groups the analgesics overall consumption per os during the first 24 hours following the joining of the episiotomy(24 hours)
  • To compare between the 3 groups the total cost of the analgesics consumption (local anaesthetic employed and analgesics per bone) during the first 24 hours following the joining of the episiotomy(24 hours)

研究者

发起方
University Hospital, Angers
申办方类型
Other Gov

研究点 (2)

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