Evaluating pain management strategies after scoliosis surgery
Analysis of Different Postoperative Analgesia Strategies Following Scoliosis Surgery: Retrospective Study
University Hospital, Strasbourg, France · NCT06194279
This study is testing different pain relief methods after scoliosis surgery to see if combining them helps patients feel better and recover faster.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 100 (estimated) |
| Ages | 16 Years and up |
| Sex | All |
| Sponsor | University Hospital, Strasbourg, France (other) |
| Locations | 1 site (Strasbourg) |
| Trial ID | NCT06194279 on ClinicalTrials.gov |
What this trial studies
This study analyzes various postoperative analgesia strategies for patients who have undergone surgery for idiopathic scoliosis. It focuses on the effectiveness of multimodal analgesia techniques, including intrathecal morphine injection and spinal erector block, to optimize pain management and enhance recovery. The research aims to determine if combining these techniques can provide better pain relief compared to traditional methods. Data will be collected from patients treated at the University Hospital in Strasbourg over a specified period.
Who should consider this trial
Good fit: Ideal candidates are patients aged over 15 who have undergone scoliosis surgery at the University Hospital in Strasbourg between January 2020 and June 2023.
Not a fit: Patients with a history of spinal surgery or those on level 3 analgesics at home may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved pain management strategies for patients recovering from scoliosis surgery.
How similar studies have performed: Previous studies have shown effectiveness in individual analgesic techniques, but the combination approach being evaluated here is novel.
Eligibility criteria
Show full inclusion / exclusion criteria
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
Where this trial is running
Strasbourg
- Service d'Anesthésie Réanimation Médecine Péri Opératoire - CHU de Strasbourg - France — Strasbourg, France (RECRUITING)
Study contacts
- Study coordinator: Fanny PLANQUART, MD
- Email: fanny.planquart@chru-strasbourg.fr
- Phone: 33 3 88 12 70 75
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions: Idiopathic Scoliosis