Influence of Analgesic Technique on Post Operative Rehabilitation After Median Laparotomy

ConditionLaparotomy
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorCentre Hospitalier Régional Metz-Thionville

About this trial

Randomized controlled trial (1:1) in two parallel groups, multicentric, open-label, comparing two locoregional anesthesia (LRA) techniques as integral parts of multimodal analgesia: the control group will benefit from epidural anesthesia, while the experimental group will benefit from bilateral placement of catheters in the sheath of the rectus abdominis muscles.

Eligibility criteria

Qualifiers

ASA (American Society of Anesthesiologists) Class I-IV adult, with programmed midline laparotomy

Have given an informed written consent

Able to read and understand french language

Affiliation to a social security system

Disqualifiers

Local anesthesic contraindication (allergy, porphyria, haemolytic anaemia, uncontrolled epilepsy, or severe cardiac conduction disorders) or TEA (coagulation disorders, progressive neurological disease, or severe spinal disorder),

Epidural analgesia contraindication

With impossibility to set up bilateral rectus sheath block

Participation in another clinical study

Trial design

Treatments tested in this trial

  • Epidural analgesia
  • Bilateral rectus sheath block
  • Laparotomy

Treatment groups

110 Participants
are divided into 2 treatment groups