Dixon MRI Imaging Histology for Predicting Postoperative Infection in Posterior Lumbar Fusion for Myasthenia Gravis
NCT ID: NCT06805643
Last Updated: 2025-02-03
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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NOT_YET_RECRUITING
1300 participants
OBSERVATIONAL
2025-02-28
2026-02-28
Brief Summary
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Detailed Description
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Conditions
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Study Design
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OTHER
RETROSPECTIVE
Study Groups
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postoperative infection
No interventions assigned to this group
Non-operative infections
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* Inclusion of patients with sarcopenia is subject to the definition and diagnostic criteria of the European Consensus on Definition and Diagnosis of Sarcopenia.
* The patient underwent posterior lumbar fusion and had a Dixon MRI scan within 2 weeks prior to surgery.
* Patients were able to understand the purpose and procedures of the study and were willing to sign an informed consent form.
* The patient's clinical consultation and follow-up information was complete.
Exclusion Criteria
* Patients with serious other medical conditions, such as heart disease, kidney disease or liver disease, which may affect their post-operative recovery.
* Patients have known immune system disorders or are on immunosuppressive therapy, which may affect their risk of infection.
* The patient has had other spinal surgery within the last 6 months.
18 Years
ALL
No
Sponsors
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The First People's Hospital of Yunnan
OTHER
Responsible Party
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Yijin Wang
doc
Central Contacts
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Other Identifiers
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KHLL2023-KY209-GZ2024-12-23
Identifier Type: -
Identifier Source: org_study_id
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