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MDT22045CSTAIL

The ailliance post-market clinical study
Source : Importé depuis le centre

Référence clinicaltrials.gov: NCT05856370
Recrutement ouvert
Dernière modification : 2025/06/10
Type de recherche

Interventionnel


Population cible

Condition médicale (spécialité visée)

Donnée non disponible

Profil des participants

Sexe(s) des participants

ALL

Source : Importé depuis le centre

Critères de sélection

Critères d'inclusion

Inclusion Criteria:

1. Subject provides written informed consent per institution and/or geographical requirements.
2. Subject is intended to receive or be treated with an eligible Medtronic Cranial and Spinal Technology (CST) device(s) (see product appendices), used alone or in combination, for a cranial and/or spinal indication(s).
3. Subject is at least 18 years of age or minimum legal age as required by local regulations.
4. Subject agrees to complete all required assessments per the Schedule of Events.

Exclusion Criteria:

1. Subject is currently enrolled or plans to enroll in concurrent drug/device/biologic trial(s) that may confound this trial's results per investigator assessment (i.e. no required intervention that could affect interpretation of all-around device safety and or performance).
2. Subject who is, or is expected to be, inaccessible for all required follow-up visits.
3. Subject with exclusion criteria required by local law.
4. Subject is considered vulnerable at the time of obtaining consent.

Source : Importé depuis le centre

Thérapie ou Intervention proposée

Cohortes
Nom Condition médicale Traitement État du recrutement
Receiving eligible Medtronic device(s) from all product groups Powered Systems, Instruments, and Imaging device(s), Advanced Energy device(s), Robotics and Navigation, Rods and Screws, Interbodies and Biologics, Spinal Tethers, and Other Spinal Hardware device(s) Donnée non disponible
  • Inconnu
  • Receiving eligible Medtronic device(s) from all product groups
    État du recrutement
    unknown
    Données à jour depuis : 10 juin 2025

    Description de l'étude

    Résumé de l'étude

    The purpose of this clinical study is to collect performance and safety data for post-market Medtronic devices indicated for cranial and/or spinal indication(s).

    Subjects are enrolled and followed postoperatively to 24 months. The Ailliance clinical study is intended to collect data congruous with routine clinical care practices.

    Source : Importé depuis le centre

    Sites

    Centres participants


    Dernière modification : 10 juin 2025
    Données à jour depuis : 12 juin
    Origine des données : clinicaltrials.gov
    Référence clinicaltrials.gov: NCT05856370