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The ApiFix MID-C System is a unidirectional expandable rod, designed to be connected unilaterally to the spine via 2 anchor points on the concave side of a scoliotic deformity above and below the apex of the major curvature to treat adolescent idiopathic scoliosis. The MID-C System is designed to act as an internal brace. A total of 10 patients, who are planned to undrego the MID-C System implantation procedure will be enrolled for the study. A 5 years follow-up post surgery will be performed for these patients in order to evaluate the long term safety and efficacy of the MID-C System.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| MID-C treatment | Experimental | Follow-up measurements during 5 years post MIC-C system implantationin order to evaluate safety and efficacy parameters. |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| MID-C System -Minimal invasive deformity correction system for the treatment of AIS | Device | A 5 years follow-up will be performed for all patients who underwent AIS repair surgery using the MID-C System. The follow-up in order to assess safety and efficacy measurments. Eligible Patients will be followed and assessed at the following time points: Immediate Post-op up to 6 weeks, 6 months, 12 months, and then annually out to 5 years post-implantation. During the study, the following rating scales and assessments will be conducted to assess the probable benefit and safety of the treatment: Physical exam,X-rays,Cobb angle measurements,Adverse Events (AEs) and Scoliosis research society (SRS-22) questionnaire: The questionnaire is commonly used to assess health related quality of life in children with AIS. |
| Measure | Description | Time Frame |
|---|---|---|
| Efficacy endpoint | Maintenance of major Cobb angle ≤ 30° 5 years post-surgery | 5 years post MID-C system implantation |
| Safety endpoint | Serious adverse events, and device or procedure-related adverse events | 5 years post MID-C system implantation |
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Inclusion Criteria:
1. Adolescent Idiopathic Scoliosis classified as Lenke Type 1 or Type 5 curves; 2.
Exclusion Criteria:
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The study is a prospective, single arm, non-randomized, new enrollment cohort study
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