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Recruiting Not applicable NCT07538141

The Hyalex MTP Study

No applicable phase (e.g. observational)
Conditions: Hallux Valgus Hallux Limitus Hallux Rigidus

Sponsor: Hyalex Orthopaedics, Inc.

trial.available_in: БГ
Overview
The HYALEX SLALOM MTP Hemiarthroplasty System consists of a synthetic implant designed to replace the distal metatarsal surface of the great toe for treatment of arthritis . The system is composed of the HYALEX MTP Implant and instrumentation. The implant consists of the HYALEX Cartilage material bonded to a titanium backing.
Who can participate
Inclusion Criteria: 1. 21-75 years; 2. Body Mass Index (BMI) ≤ 38; 3. Degenerative or post-traumatic arthritis of the first metatarsal joint with ICRS grade 2, 3, or 4; 4. Pre-operative VAS pain score of \>40; 5. Presence of good bone stock, without need for bone graft Exclusion Criteria: 1. Known allergy to polyurethanes, bone cement, acrylic, or titanium; 2. Due to anatomy and/or lesion location, inability to position the implant flush or slightly proud relative to the articular surface precluding proper device placement; 3. Lack of 2mm of vital bone on all sides of implant site; 4. Cartilage lesions on the phalanx of ICRS Grade 3 - 4 opposite the lesion intended for treatment; 5. Additional ipsilateral lower limb (hip, knee, ankle, or foot) pathology that requires active treatment (e.g., surgery, brace); 6. Bilateral degenerative or post-traumatic arthritis of the MTP joints that would require simultaneous treatment of both MTP joints; 7. Previous cheilectomy resulting in inadequate bone stock; 8. Diagnosis of gout; 9. Hallux varus to any degree or hallux valgus \>20; 10. Hyper mobility at proximal metatarsal joint; 11. Interphalangeal angle \>15
Interventions
MTP Hemiarthroplasty
DEVICE
Locations 1
Poland (1)
SPORTO
Lodz
Technical details
Status
Recruiting
Phase
Not applicable
Study type
INTERVENTIONAL
Sex
Male and female
Minimum age
21 Years
Maximum age
75 Years
Healthy volunteers
No
Start date
01.10.2025
Completion date
31.12.2027
Registry ID
NCT07538141
Source
clinicaltrials.gov
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