Postoperative Pain in Neonates After Abdominal Surgery Using Quadratus Lumborum Block
NCT ID: NCT03203031
Last Updated: 2020-07-08
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
10 participants
OBSERVATIONAL
2017-06-30
2021-10-01
Brief Summary
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Detailed Description
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Conditions
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Study Design
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CASE_ONLY
PROSPECTIVE
Study Groups
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Neonates with abdominal surgery and quadratus lumborum block
0-6 months children with abdominal surgery. After standard induction of general anesthesia, patients will receive 0.5 ml/kg of ropivacaine (2 mg/ml) in a quadratus lumborum block. Ultrasonography will be used to guide the injection. In the postoperative period, pain scores and analgesics consumption will be recorded until the 48th hour post surgery.
General anesthesia
Standard general anesthesia
Quadratus lumborum block
Guided by ultrasonography, injection of 0.5 ml/kg of ropivacaine (2 mg/ml) between the quadratus lumborum muscle and the internal oblique muscle, before skin incision
Interventions
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General anesthesia
Standard general anesthesia
Quadratus lumborum block
Guided by ultrasonography, injection of 0.5 ml/kg of ropivacaine (2 mg/ml) between the quadratus lumborum muscle and the internal oblique muscle, before skin incision
Eligibility Criteria
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Inclusion Criteria
* spontaneously breathing before the procedure
Exclusion Criteria
* mechanical ventilation before the procedure
6 Months
ALL
No
Sponsors
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Hôpital Armand Trousseau
OTHER
Responsible Party
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Pr Isabelle CONSTANT
Professor
Principal Investigators
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Isabelle Constant, MD-PHD
Role: STUDY_DIRECTOR
Hopital Armand Trousseau, Université Paris 6, Département d'anesthésie
Locations
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Hopital Armand Trousseau
Paris, , France
Countries
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Other Identifiers
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CARRE DES LOMBES
Identifier Type: -
Identifier Source: org_study_id
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