The aims of this Discoid Meniscus (DiMe) project are to analyze DM tears characteristics in the pediatric European population to describe current treatment options in symptomatic DM, and to evaluate clinical outcomes. To reach these objectives, a prospective database including symptomatic DM and variables associated with DM characteristics, type of tears, treatment, imaging, and clinical follow-up will be implemented. Data collection platform will provide future studies to understand the best treatment option for skeletally immature patient with symptomatic DM according to their history and lesion characteristics.
This is a multicentric international prospective cohort study. All eligible consecutive patients will be identified prospectively by the local participating clinical teams according to Inclusion/Exclusion Criteria. Prospective data entry is mandatory. Data collection will be conducted in three phases: * Phase 1 will register patients to the study, document symptomatic DM, collect the details of patient demographics, sport characteristics, PROMS, imaging classification and consent of the patient's legal representatives. Once the patient has reached the age of majority, the date of his/her own consent will be recorded. * Phase 2 will register surgical treatment and arthroscopic video and photographs collected during surgery, collect intraoperative DM instability, arthroscopic classification, and surgical details. Post-operative complication will also be collected. * Phase 3 will collect short-, medium- and long-term outcome data. Short follow-up data collection will plan at 1 month follow-up then 3 and 6-months follow-up. Then annual data collection will be performed. The foreseen timeframe of follow-up will be 15 years for each patient. At the end of the 15-year follow-up, the data will be stored for an additional 10 years before being deleted. Data will be recorded if the patients are willing to comply with the annual data collection. Should the DiMe Project be terminated at one stage, the data will be stored for 10 years after termination of the project before being deleted.
Study Type
OBSERVATIONAL
Enrollment
500
Universitair Ziekenhuis
Leuven, Belgium
NOT_YET_RECRUITINGOulu University Hospital,
Oulu, Finland
NOT_YET_RECRUITINGCHU Grenoble
Grenoble, France
NOT_YET_RECRUITINGClinique Rive Gauche
Toulouse, France
NOT_YET_RECRUITINGDepartment of Orthopaedic Surgery, Hôpital des Enfants, CHU de Toulouse
Toulouse, France
NOT_YET_RECRUITINGPoliclinico San Pietro
Bergamo, BG, Italy
NOT_YET_RECRUITINGASST Monza - Ospedale San Gerardo
Monza, Italy
RECRUITINGDepartment of Pediatric Orthopaedics, Hospital Pediátrico de -Coimbra
Coimbra, Portugal
NOT_YET_RECRUITINGHospital Cuf Descobertas
Lisbon, Portugal
NOT_YET_RECRUITINGCentre hospitalier universitaire vaudois (CHUV)
Lausanne, Switzerland
NOT_YET_RECRUITING...and 2 more locations
Pedi-IKDC (0-100) among the three types of DM according to Ahn classification.
Time frame: Enrollment period (approximately 5 years)
Time to return to sport (months) among the three types of DM tear according to Ahn classification.
Time frame: Entire study duration (approximately 20 years)
Tegner activity level scale (0-10) among the three types of DM tear according to Ahn classification.
Tegner activity level scale:0=Sick leave or disability pension because of knee problems 10=Competitive sports Soccer - national and international elite
Time frame: Entire study duration (approximately 20 years)
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