CClinicalTrials.gg
Status unknownNCT05510011Updated Aug 22, 2022

Allograft and Tantalum Cone Reconstruction in TKA Revision

An observational study in Tantalum, Bone Loss and Allograft, sponsored by University Hospital, Montpellier. Status unknown at 1 site in France. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2022-08-22.

Sponsored by University Hospital, Montpellier · Observational

The sponsor has not verified this record recently (last verified Jan 2022), so the status shown — last known as Recruiting — may be out of date.
Study type
Observational
Model
Cohort
Time perspective
Retrospective
Enrollment
76
Ages
18 Years and older
Sex
All
01

Study summary

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

Study of radiological and clinical outcomes.

02

Conditions studied

  • Tantalum
  • Bone Loss
  • Allograft

Keywords

  • Tantalum
  • Allograft
  • TKA revision using tantalum cone and/or allograft
03

In context

Lead sponsor

University Hospital, Montpellier is the lead sponsor of 1,244 studies on the registry; 225 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Probability sample

Study population

Pregnant women attending for 3rd timester scan

Inclusion criteria

  • > 18 years old
  • TKA revision using tantalum cone or allograft

Exclusion criteria

Exclusion criteria:

  • \<18 years old
  • no reconstruction used in TKA revision
05

Study design

Observational model
Cohort
Time perspective
Retrospective
Enrollment
76 participants (estimated)
Patient registry
No
06

What researchers measure

Primary outcomes

  1. Rate of Survivorship of the implant

    Survivorship of the implant

    Time frame: day 1

07

Study locations

1 of 1 sites recruiting
08

References and documents

Individual participant data

Plan to share: Undecided — NC

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 22, 2022, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05510011
Lead sponsor
University Hospital, Montpellier
Responsible party
Sponsor
First posted
Aug 22, 2022
Start date
Jan 1, 2022
Primary completion
Feb 20, 2023 (estimated)
Completion
Feb 21, 2023 (estimated)
Last update
Aug 22, 2022

Study contacts

Louis DAGNEAUX, PHU
Contact
f-fuchs@chu-montpellier.fr
04 67 33 09 80 ext. 33
Elias BOUGAUD, Resident
Contact
e-bougaud@chu-montpellier.fr
682500767 ext. 33
Louis DAGNEAUX, PHU
study director · University Hospital, Montpellier

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Jan 2022. You cannot join it, but the record below documents what was studied.

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