Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
40 participants
OBSERVATIONAL
2015-12-31
2018-09-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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CASE_CONTROL
PROSPECTIVE
Study Groups
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Study group
Patients undergoing forefoot reconstruction of hallux valgus or hallux rigidus
Forefoot surgery
Forefoot surgery (Chevron, Scarf, Lapidus, Arthrodesis)
Control group
Healthy volunteers (Students)
No interventions assigned to this group
Interventions
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Forefoot surgery
Forefoot surgery (Chevron, Scarf, Lapidus, Arthrodesis)
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
18 Years
ALL
Yes
Sponsors
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Technical University of Munich
OTHER
Responsible Party
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Harrasser
Dr.
Principal Investigators
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Rüdiger Eisenhart-Rothe, Prof.
Role: STUDY_DIRECTOR
Head of Orthopedic Dept.
Locations
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Klinikum rechts der Isar
Munich, Bavaria, Germany
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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10111
Identifier Type: -
Identifier Source: org_study_id
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