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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05510011
Other study ID # RECHMPL22_0013
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date January 1, 2022
Est. completion date February 21, 2023

Study information

Verified date January 2022
Source University Hospital, Montpellier
Contact Louis DAGNEAUX, PHU
Phone 04 67 33 09 80
Email f-fuchs@chu-montpellier.fr
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

A new surgical technique of reconstruction for bone loss in TKA revision using tantalum cone and allograft. Study of radiological and clinical outcomes.


Recruitment information / eligibility

Status Recruiting
Enrollment 76
Est. completion date February 21, 2023
Est. primary completion date February 20, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion criteria: - > 18 years old - TKA revision using tantalum cone or allograft Exclusion criteria: - <18 years old - no reconstruction used in TKA revision

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
France Uhmontpellier Montpellier

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Montpellier

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Rate of Survivorship of the implant Survivorship of the implant day 1
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