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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RECRUITING
1000000 participants
OBSERVATIONAL
2017-01-31
2100-01-31
Brief Summary
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Objective: The main objective of this registry is to collect patient characteristics and treatment parameters together with data from the questionnaires in a database. This knee registry can be used for future research questions.
Study design: This is a longitudinal observational registry.
Study population: All patients that visit the Mobility Clinic will be asked to participate in the knee registry. Patients that meet one or more of the following criteria will be excluded: are below the age of 16, not able or willing to sign the broad consent form, not being able to read and understand Dutch language, or receiving medical treatment for their knee elsewhere.
Main study parameters/endpoints: Data will be collected for future research for which the purpose is not known at this time. When new research will be conducted, study parameters will be set. A study application has to be submitted to the institutional ethical review board of the University Medical Center Utrecht. Patients do not need to be asked permission for the use of their data for each study individually. Only when additional information is needed.
Nature and extent of the burden and risks associated with participation, benefit and group relatedness: The burden for patients to participate in this registry is minimal and consists of time. Any future results may be beneficial for patients. Participation or refusal to participate in the registry has no consequences for their treatment.
Detailed Description
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Conditions
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Keywords
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Knee registry patients
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* Able to read and understand Dutch language;
* Is able and willing to signs the broad consent form.
Exclusion Criteria
* Receives treatment elsewhere.
ALL
No
Sponsors
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UMC Utrecht
OTHER
Responsible Party
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R.J.H. Custers
Principal Investigator
Principal Investigators
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Roel Custers, Dr
Role: PRINCIPAL_INVESTIGATOR
Orthopedic surgeon
Locations
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University Medical Center Utrecht
Utrecht, , Netherlands
Countries
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Central Contacts
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Facility Contacts
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Roel Custers, Dr
Role: primary
Related Links
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Het knieregister: register voor kniebehandelingen
Knee joint distraction in regular care for treatment of knee osteoarthritis: A comparison with clinical trial data.
ICRS Patient Registry
Reduction of pin tract infections during external fixation using cadexomer iodine
Other Identifiers
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17-005
Identifier Type: -
Identifier Source: org_study_id