The Recovery after Achilles Tendon Rupture: an Exploratory Cohort Study
Completed
- Conditions
- Achilles tendon rupture10043237
- Registration Number
- NL-OMON45706
- Lead Sponsor
- Sportgeneeskunde
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 50
Inclusion Criteria
-Be older than 18 years of age at the time of inclusion
-Have been clinically diagnosed with an Achilles tendon rupture and have been treated less than 3 months ago at the UMCG, Martini Hospital or MCL
-Give written informed consent
Exclusion Criteria
-Unable to understand Dutch
-Inability to perform and or understand the tests and/or questionnaires
Study & Design
- Study Type
- Observational non invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method
Related Research Topics
Explore scientific publications, clinical data analysis, treatment approaches, and expert-compiled information related to the mechanisms and outcomes of this trial. Click any topic for comprehensive research insights.
What molecular pathways are involved in Achilles tendon rupture recovery as studied in NL-OMON45706?
How does NL-OMON45706's non-surgical approach compare to surgical repair in Achilles tendon rupture recovery?
Which biomarkers predict functional recovery outcomes in Achilles tendon rupture patients from NL-OMON45706?
What are the common adverse events during Achilles tendon rupture rehabilitation in NL-OMON45706 and their management?
How do adjunct therapies like PRP or stem cells affect recovery compared to standard care in Achilles tendon rupture studies?