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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00132587
Other study ID # 2003.313
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date March 2004
Est. completion date March 2007

Study information

Verified date June 2008
Source Hospices Civils de Lyon
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of the study is to analyse and to compare the quality of fixation of a femoral implant with or without cement.

One hundred thirty patients will be operated on and included with 2 groups, the first one with TKA all cemented and the second one with TKA with a cementless femoral implant. The study criteria include the IKS (International Knee Society) score and the analysis of a radiolucent line at the femur.

Patients will be reviewed at 2, 6 and 12 months.


Recruitment information / eligibility

Status Completed
Enrollment 130
Est. completion date March 2007
Est. primary completion date December 2006
Accepts healthy volunteers No
Gender All
Age group 50 Years to 90 Years
Eligibility Inclusion Criteria:

- Osteoarthritis (medial and/or lateral femoro-tibial arthritis and/or patellofemoral arthritis)

- Indication of surgical treatment by total knee arthroplasty

- Age between 50 and 90 years

- Acceptance and signature to participate

Exclusion Criteria:

- Rheumatoid or other inflammatory arthritis

- Association with other surgical procedure (osteotomy)

- Range of motion inferior to 90°

- Previous knee surgery (except arthroscopy)

Study Design


Related Conditions & MeSH terms


Intervention

Device:
cement Palacos R40 and LV40


Locations

Country Name City State
France Hôpital de la Croix-Rousse Lyon

Sponsors (1)

Lead Sponsor Collaborator
Hospices Civils de Lyon

Country where clinical trial is conducted

France, 

References & Publications (1)

Demey G, Servien E, Pinaroli A, Lustig S, Aït Si Selmi T, Neyret P. The influence of femoral cementing on perioperative blood loss in total knee arthroplasty: a prospective randomized study. J Bone Joint Surg Am. 2010 Mar;92(3):536-41. doi: 10.2106/JBJS.H — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary IKS (International Knee Society) score at 12 months
Secondary Analysis of femoral radiolucent line at the X-rays (profile and anterior-posterior [AP] view) at 12 months
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