Skip to main content
Clinical Trials/NL-OMON21786
NL-OMON21786
Recruiting
Not Applicable

Safety and effectiveness evaluation of the Minimal Invasive Deformity Correction (MID-C) System in adolescent idiopathic scoliosis

VU University Medical Center, Amsterdam, The Netherlands0 sites33 target enrollmentTBD

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Surgical treatment of adolescent idiopathic scoliosis (AIS).
Sponsor
VU University Medical Center, Amsterdam, The Netherlands
Enrollment
33
Status
Recruiting
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional

Investigators

Sponsor
VU University Medical Center, Amsterdam, The Netherlands

Eligibility Criteria

Inclusion Criteria

  • 1\. Adolescent AIS patients (12 years \- 17 years old);
  • 2\. Standing X\-ray: 40 to 55 degrees Cobb angle, Lenke type 1 or 5, Risser stage 1\-4;

Exclusion Criteria

  • 1\.Other non\-idiopathic form of scoliosis;
  • 2\.Primary curve Cobb angle \>55 degrees;

Outcomes

Primary Outcomes

Not specified

Similar Trials

Completed
Not Applicable
Evaluation of the safety and effectiveness of the MID-C/ApiFix system in adolescent idiopathic scoliosis.Spinal curvature1002837710005944
NL-OMON43676Vrije Universiteit Medisch Centrum33
Not yet recruiting
Phase 4
euroEPO in mild-moderate Alzheimer's disease amnesic variantmild-moderate Alzheimer's diseaseAlzheimer DiseaseDementiaBrain DiseasesCentral Nervous System DiseasesNervous System DiseasesTauopathiesNeurodegenerative DiseasesNeurocognitive DisordersMental Disorders
RPCEC00000410Center of Molecular Immunology (CIM)1,456
Active, not recruiting
Not Applicable
Safety and effectiveness clinical evaluation of the range of injectable medical devices HYDRAGEL C in facial aesthetic treatmentSubjects across groups present with moderate to severe facial aesthetic concerns, including peri-oral lines, nasolabial folds, lip volume deficits, and cheeks/cheekbones volume deficit, as gauged by various dermatological scalesSkin and Connective Tissue Diseases
ISRCTN13586698ouna Aesthetics75
Active, not recruiting
Not Applicable
Clinical study to evaluate the safety and effectiveness of the use of two hyaluronic acid injectable products (Perfectha® Derm Lidocaine and Perfectha® Deep Lidocaine) in the treatment of lipsFor Perfectha® Derm Lidocaine: very thin to thin lip volume and with lip contour somewhat well-defined to poorly definedfor Perfectha® Deep Lidocaine: thin to moderate lip volumeNot Applicable
ISRCTN72858148Sinclair Pharma68
Completed
Not Applicable
Evaluation of the safety and efficacy of the Optimizer™ II and III systems with active fixation leads in subjects with heart failure resulting from systolic dysfunctioHeart failureCirculatory System
ISRCTN16213127Impulse Dynamics Inc. (USA)250