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Position HTO Multicenter NIS

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Aesculap

Status

Completed

Conditions

Medial Monocompartmental Osteoarthritis of the Knee

Treatments

Device: Position HTO system

Study type

Observational

Funder types

Industry

Identifiers

NCT00889304
AAG-O-H-0702

Details and patient eligibility

About

Evaluation of the Position HTO system in patients with unicompartmental medial arthrosis after open wedge high tibial osteotomy

Enrollment

221 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion: Varus deformity between 0 - 20°, Isolated medial arthrosis ≥ level 2 (K&L) OR a congenital deformity OR chondromalacia ≥ level 2 (ICRS), Lateral cartilaginous tissue damage ≤ level 1(K&L), Intact lateral meniscus, Age ≥ 18 years, Range of Motion at least 0° - 0° - 130°, Patella/ sliding plane without signifikant signs of arthrosis, Stable joint OR possibility of intraoperative balancing of the tendon tension;

Exclusion: Clinically relevant disorders of bone metabolism, Aktive infection, Adipositas (BMI ≥ 35), Rheumatoid arthritis, Osteomyelitis in the tibia, No availibility for follow-up examinations

Trial design

221 participants in 1 patient group

A
Description:
HTO cohort
Treatment:
Device: Position HTO system

Trial contacts and locations

5

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Data sourced from clinicaltrials.gov

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