ong-Term Outcomes after Surgical Treatment for Foot Injuries - A Multicenter Prospective Cohort Study
- Conditions
- Foot FracturesFoot InjuriesFoot DislocationsLisfrancChopartPosttraumatic Sequealae of Foot InjuriesPosttraumatic ArthritisVoetfracturenVoetletselsDislocaties van de VoetPosttraumatische Gevolgen van Voetletsels
- Registration Number
- NL-OMON29244
- Lead Sponsor
- niversitair Medisch Centrum Utrecht
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- Not specified
- Target Recruitment
- 200
Inclusion Criteria
In order to be eligible to participate in this study, a subject must be undergoing operative treatment for at least one (posttraumatic sequelae of a) traumatic foot fracture and/or dislocation at one of the participating centers. All subjects must be at least 18 years of age at the time of surgery.
Exclusion Criteria
A potential subject who meets any of the following criteria will be excluded from participation in this study:
-Initial surgical treatment elsewhere (in case of an acute injury)
Study & Design
- Study Type
- Observational non invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Health-related quality of life as measured using the EQ-5D-3
- Secondary Outcome Measures
Name Time Method -Functional outcome as measured using the AOFAS Forefoot, Midfoot, and/or Ankle-Hindfoot scale<br /><br>-Return to work<br /><br>-Return to sports<br /><br>-Complication after surgery; deep infection, superficial infection, wound healing disorder, thromboembolic complication, implant failure, re-fracture and/or other<br /><br>-Need for secondary surgery (with indication, also if performed at outside facility)<br /><br>-Implant removal; yes or no and reason if positive<br /><br>-Transfer (L2 to L1 and vice versa)<br /><br>-Surgical team composition (surgeon(s) from hosting facility only, combination of surgeons)