Outcome EnduRo Versus LINK SL Rotating Hinge Knee
Sponsor
Orthopaedische Klinik Koenig-Ludwig-Haus (Other)
Overall Status
Unknown status
CT.gov ID
NCT01952938
Collaborator
(none)
50
1
Study Details
Study Description
Brief Summary
Randomized clinical outcome study of two rotating hinge knee prosthesis in knee surgery. Hypothesis: No difference in the clinical outcome for 1 year after the operation. Clinical follow-ups at 3, 10, 90 and 360 days after surgery. Measurement of clinical parameters
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
Study Design
Study Type:
Observational [Patient Registry]
Anticipated Enrollment
:
50 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Study Start Date
:
Jul 1, 2012
Anticipated Primary Completion Date
:
Jul 1, 2014
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| LINK SL Patients |
Procedure: LINK SL versus EnduRo
|
| EnduRo Patients |
Procedure: LINK SL versus EnduRo
|
Outcome Measures
Primary Outcome Measures
- Oxford knee score [one year]
Eligibility Criteria
Criteria
Ages Eligible for Study:
N/A
and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
- rotating hinge knee indicated
Exclusion Criteria:
-
infection,
-
malignant tumor,
-
rheumatism
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Orthopeadische Klinik KLH | Wuerzburg | Bavaria | Germany | 97074 |
Sponsors and Collaborators
- Orthopaedische Klinik Koenig-Ludwig-Haus
Investigators
None specified.Study Documents (Full-Text)
None provided.More Information
Publications
None provided.Responsible Party:
Orthopaedische Klinik Koenig-Ludwig-Haus
ClinicalTrials.gov Identifier:
NCT01952938
Other Study ID Numbers:
- AAG-I-H-1112
First Posted:
Sep 30, 2013
Last Update Posted:
Sep 30, 2013
Last Verified:
Sep 1, 2013
Keywords provided by Orthopaedische Klinik Koenig-Ludwig-Haus
Additional relevant MeSH terms: