Knee registry for patients receiving knee treatment
Collecting Diagnostic, Treatment and Follow-up Data on Knee Treatments.
This study collects information from patients getting knee treatment at a clinic to see how their knee function, pain, and mobility change before and after treatment.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 1000000 (estimated) |
| Sex | All |
| Sponsor | UMC Utrecht Academic / other |
| Locations | 1 site (Utrecht) |
| Trial ID | NCT04364334 on ClinicalTrials.gov |
What this trial studies
This observational registry collects data on patients visiting the Mobility Clinic at the University Medical Center Utrecht for orthopedic knee treatment. It gathers patient characteristics, treatment parameters, and responses to questionnaires regarding knee function, pain, and mobility before and after treatment. The aim is to create a comprehensive database that can be utilized for future research questions related to knee pathology. The study involves all patients receiving treatment at the clinic, ensuring a broad representation of knee-related conditions.
Who should consider this trial
Good fit: Ideal candidates are patients aged 16 and older receiving orthopedic knee treatment at UMC Utrecht who can read and understand Dutch.
Not a fit: Patients who are receiving knee treatment elsewhere or refuse treatment will not benefit from this registry.
Why it matters
Potential benefit: If successful, this registry could enhance understanding of knee treatments and improve patient outcomes through data-driven insights.
How similar studies have performed: Other observational registries have shown success in improving treatment outcomes and understanding patient needs, indicating a promising approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Receives orthopaedic knee surgery or conservative knee treatment (advice, physiotherapy, injections etc) at the UMC Utrecht; * Able to read and understand Dutch language; * Is able and willing to signs the broad consent form. Exclusion Criteria: * Receives no treatment (refusal of surgery or treatment); * Receives treatment elsewhere.
Where this trial is running
Utrecht
- University Medical Center Utrecht — Utrecht, Netherlands (Recruiting)
Study contacts
- Principal investigator: Roel Custers, Dr — Orthopedic surgeon
- Study coordinator: Linda Kornegoor, MSc
- Email: l.kornegoor@umcutrecht.nl
- Phone: 088 75 69349
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.