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Optimization of a Tool for Predicting Postoperative Clinical Evolution After Lumbar Surgery

NCT05166018 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 119

Last updated 2023-02-10

No results posted yet for this study

Summary

The objective of the study is the establishment, optimization and prospective evaluation of a digital predictive platform capable of providing for each lumbar spine operated patient a clinical predictive status: Patient green (success) orange (treatment failure ), red patient (complication) in order to optimize his medical care up to 6 months.

Conditions

  • Spine Disease
  • Spinal Fusion
  • Surgery
  • Spine Degeneration

Interventions

DIAGNOSTIC_TEST

SuMO Patient

The current study is interventional insofar as the patient is collecting all of his socio-medical information. The analysis of the data provided by the patient makes it possible to establish a long-term prognosis for the patient but does not in itself constitute a parallel medical approach. SUMO allows the surgeon to transmit post-operative advice developed by the surgeons themselves.

Sponsors & Collaborators

  • Ramsay Générale de Santé

    collaborator OTHER

  • Elsan

    collaborator OTHER

  • Malakoff-Humanis

    collaborator UNKNOWN

  • Cortexx Medical Intelligence

    lead INDUSTRY

Study Design

Allocation
NA
Purpose
DIAGNOSTIC
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-06-15
Primary Completion
2022-06-30
Completion
2022-12-30

Countries

  • France

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05166018 on ClinicalTrials.gov