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Results of the Tactys Implant in Proximal Interphalangeal Joint Arthroplasty

Proximal Interphalangeal Joint Arthroplasty With the TACTYS® Prosthesis : Clinical and Radiographic Results at Medium Term.

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04658459
Enrollment
100
Registered
2020-12-08
Start date
2015-01-01
Completion date
2021-07-31
Last updated
2020-12-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Interphalangeal; Osteoarthritis, Proximal (Bouchard)

Keywords

tactys prosthesis

Brief summary

Study at middle term of the functional and radiographic results of proximal interphalangeal joint arthroplasty with the Tactys prothesis. The aim is to evaluate if the short term results are maintained in time.

Detailed description

The inclusion criteria is any patient who has undergone a proximal interphalangeal joint arthroplasty with the Tactys prothesis between january 2015 to january 2020 in the Centre Chirurgical Emile Gallé in Nancy. The functional results evaluated are range of motion, force, pain, functional score as Quick DASH and the radiological one are clinodactyly, periprosthetic ossifications and loosening, dislocation and implant subsidence. Data is registered from the medical folder of every patient.

Interventions

PROCEDUREProximal Interphalangeal Joint Arthroplasty with the Tactys Prosthesis

Sponsors

Central Hospital, Nancy, France
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* one or more proximal interphalangeal joint arthroplasty of long fingers with the Tactys prosthesis * between january 2015 to january 2020 * major * centre chirurgical emile gallé, centre hospitalier régional universitaire de Nancy

Exclusion criteria

* minor

Design outcomes

Primary

MeasureTime frameDescription
range of motion in degreesminimal one year post-operativemeasurement of range of motion in degrees
force in kilogramsminimal one year post-operativemeasurement of force with jamar and pinch tests in kilograms
pain with the digital pain scaleminimal one year post-operativemeasurement of pain with the digital pain scale to zero to ten
functional score with the Quick DASHminimal one year post-operativemeasurement of the quick-DASH functional score to zeo to hundred

Secondary

MeasureTime frameDescription
register the complication and their apparition in timeminimal one year post-operative
assess satisfactionminimal one year post-operativeassess the patient's satisfaction : very satisfied, satisfied, moderate, not satisfied

Countries

France

Contacts

Primary ContactAude LOZANO, resident
a.lozano@chru-nancy.fr0611434813

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026