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NCT06194279 Clinical Trial

Analysis of Different Postoperative Analgesia Strategies Following Scoliosis Surgery

Idiopathic Scoliosis Clinical Trial

— SAPOS  

Official title:
Analysis of Different Postoperative Analgesia Strategies Following Scoliosis Surgery: Retrospective Study

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT06194279
Other study ID # 8961
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date June 19, 2023
Est. completion date June 2024

Study information
Verified date December 2023
Source University Hospital, Strasbourg, France
Contact Fanny PLANQUART, MD
Phone 33 3 88 12 70 75
Email fanny.planquart@chru-strasbourg.fr
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Idiopathic scoliosis surgery is a major surgery, causing significant post-operative pain which can have a significant impact, both for the patient and for society. Different analgesic strategies have emerged in recent years, within the framework of multimodal analgesia including systemic analgesics, but also axial or peripheral loco-regional anesthesia (LRA). These techniques are integrated into the recommendations of learned societies, aimed at optimizing the post-operative rehabilitation of patients. If intrathecal morphine injection (ITM) and spinal erector block (ESPB) have already shown their effectiveness in reducing postoperative pain, the combination of these techniques can have a real benefit in major spinal surgery. , and has not yet been studied.

Recruitment information / eligibility
Status Recruiting
Enrollment 100
Est. completion date June 2024
Est. primary completion date June 2024
Accepts healthy volunteers
Gender All
Age group 16 Years and older
Eligibility Inclusion Criteria: - Patient aged > 15 years - Patient who underwent scoliosis surgery by the spine surgery team at Hautepierre hospital between January 1, 2020 and June 30, 2023 - Patient or holder of parental authority not opposing the reuse of their data for scientific research purposes Exclusion Criteria: - Oral or written refusal of the patient (or the holder of parental authority) to reuse their data for scientific research purposes - History of spinal surgery - Level 3 analgesics at home - Protection of justice, titular or curatorship

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
France Service d'Anesthésie Réanimation Médecine Péri Opératoire - CHU de Strasbourg - France Strasbourg

Sponsors (1)
Lead Sponsor Collaborator
University Hospital, Strasbourg, France

Country where clinical trial is conducted

France, 

Outcome
Type Measure Description Time frame Safety issue
Primary Morphine dose administered 24 hours post-operative The aim of this retrospective study is to compare the different analgesic strategies postoperatively after scoliosis surgery 24 hours post-operative
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