Return to Cross Country Skiing and Other Physical Activities After Arthrodesis of the First Metatarsophalangeal Joint
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Arthrodesis.
- Who it may be relevant to
- Registry conditions: Hallux Rigidus, Hallux Valgus. Basic parameters: 18 years — 60 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Center list to be confirmed — check the primary protocol.
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Official title
Retur Til Fysisk Aktivitet Etter Avstivning av stortåens Grunnledd
Overview
Patients who have undergone arthrodesis of the first metatarsophalangeal joint due to hallux valgus or hallux rigidus are invited to participate in this study, which aims to investigate how the foot functions after this operation. Patients between 18 and 60 years of age at the time of surgery are eligible to participate. Questionnaires will be distributed to assess current sports function compared with function prior to surgery. Particular focus will be placed on function during cross-country skiing.
Interventions
- Procedure Arthrodesis
Arhtrodesis of the first metatarsophalangeal joint
Primary outcome measures
- Return to Cross country skiing [Time frame: At least 1 year after surgery]
Eligibility criteria
Inclusion criteria
- Patients who has underwent arthrodesis of the first metatarsofalangeal joint because of hallux rigidus or severe hallux valgus
- Patients at age 18-60 at the date of surgery
- At least one year follow-up, and maximum 5 years since surgery.
Exclusion criteria
- Non-Norwegian-speaking patients.
- Impaired walking function.
- Inability to cooperate.
- Concomitant osteotomy of other metatarsals.
- Revision arthrodeses.
- Patients undergoing follow-up or evaluation for pseudoarthrosis.
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: Yes
Study design
- Observational model
- Cohort
Study locations
Center list to be confirmed — check the primary protocol.
Identifiers
NCT: NCT07610330 · 980644