Debridement of the MTP1 cartillage lesion and microfracture
Debridement of the MTP1 cartillage lesion and microfracture: Patients with a MTP1 cartillage lesion \> grade I (based on based on the ICRS scale and an MS HoloLens measurement) randomised in the treatment group will be treated with debridement and microfracture
Study summary
The aim of this study is to investigate the point or nonsense of treating cartilage lesions at the level of the first metatarsophalane joint. To date, no clear guidelines have been found in the literature with regard to the treatment of cartilage lesions at the MTP I joint during corrective surgery for hallux valgus, nor has it been investigated whether this can have an effect on the clinical outcome.
Eligibility
Sex
ALL
Min age
30 Years
Max age
60 Years
Healthy volunteers
No
Inclusion Criteria:
* hallux valgus
Exclusion Criteria:
* younger than 30 years, older than 60 years
* extra pathologies other than hallux valgus
Primary outcome measure(s)
Change in AOFAS — 10 days, 5 weeks, 4 months, 1 year American Orthopaedic Foot and Ankle Society (AOFAS) score - combines a clinician-reported and a patient-reported part for measuring the outcome of treatment in patients who sustained a complex hindfoot injury based on pain, function and alignment: 0 (bad outcome) to 100 (very good outcome)
Change in SF36 — 10 days, 5 weeks, 4 months, 1 year Short Form 36 (SF-36) Health Survey - consists of eight scaled scores, which are the weighted sums of the questions in their section. Each scale is directly transformed into a 0-100 scale on the assumption that each question carries equal weight. The lower the score the more disability. The higher the score the less disability i.e., a score of zero is equivalent to maximum disability and a score of 100 is equivalent to no disability.
Change in VAS pain — 10 days, 5 weeks, 4 months, 1 year Visual Analogue Scale pain score - 0 (no pain) to 10 (worse pain)
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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