Achilles tendon surgery - functionality after treatment of infection - a preliminary study with query of patient-reported outcome data (PROM).
Recruiting
- Conditions
- S86.0Injury of Achilles tendon
- Registration Number
- DRKS00031755
- Lead Sponsor
- BG Klinikum Hamburg
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 50
Inclusion Criteria
Index procedure performed by 12/31/2019.
Documented performance of a partial or complete Achilles tendon resection at BGKH for any indication without performing a secondary plastic.
Presentation of a signed declaration of consent for the scientific evaluation of patient data assigned to the treatment in question.
Exclusion Criteria
Patients who do not have an independently signed consent for data use (e.g., signature by relatives due to impaired cognitive function).
Study & Design
- Study Type
- observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method achieved function of the Achilles tendon
- Secondary Outcome Measures
Name Time Method It is not a controlled study or a regulatory trial. Therefore, primary or secondary outcome measures in the conventional sense do not exist. A treatment cohort of a hospital over a period of 10 years is considered. The aim is to evaluate the maximum possible number of data sets, which are limited only by the inclusion/exclusion factors. While primarily the achieved function of the Achilles tendon is put in relation to the other recorded items, a description of the study population as well as a detailed evaluation of the recorded complications and the description of the factors influencing the occurrence of a complication are also secondary. factors influencing the occurrence of a complication.<br>