Skip to main content
MedPath Trial logoMedPath TrialMedPath Trial Home
Clinical Trials/NCT06338566
NCT06338566Not yet recruitingNot Applicable

Prospective Follow-up of Functional, Bone and Septic Results of Ankle Arthrodesis With Transplanted Nail

Direction Centrale du Service de Santé des Armées0 sites20 target enrollmentStarted: March 2024Last updated:
Share to TwitterShare to FacebookShare to LinkedInShare to Reddit
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Not yet recruiting
Sponsor
Enrollment
20
Primary Endpoint
bony outcome of transcalcaneal nailing
Study OverviewStudy DesignEligibility CriteriaOutcomesInvestigatorsRecords & IdentifiersSimilar Trials

Study Overview

Brief Summary

The goal of this prospective, single-center observational study is to describe the functional outcome of the surgical procedure in patient who undergone transplanted centromedullary nailing in the septic setting.

Patients will be asked to complete a questionnaire during follow-up consultations.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to 80 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Patient >18 years
  • •having undergone septic nailing in the operating theatre
  • •with social security coverage

Exclusion Criteria

  • •Patient with 6-month follow-up not possible (medical wandering, transient patient),
  • •Patient who has benefited from another means of osteosynthesis
  • •Patients whose long-term return to weight-bearing will not be possible for reasons other than ankle arthrodesis surgery.
  • •Persons able to give consent but unable to read or write French
  • •Opposes participation in the study
  • •Patients whose cognitive capacity does not allow them to answer questionnaires

Outcomes

Primary Outcomes

bony outcome of transcalcaneal nailing

Time Frame: up to 6 months

percentage of patients with aseptic consolidation at 6 months post-op

Secondary Outcomes

  • functional result of the procedure(up to 6 months)

Investigators

Sponsor
Direction Centrale du Service de Santé des Armées
Sponsor Class
Other
Responsible Party
Sponsor

Similar Trials

Completed
Not Applicable
Results of a New Fully Tapered Implant at One YearImplant Site Reaction
NCT05187143University of Santiago de Compostela30
Terminated
Not Applicable
OLIF25™ /OLIF51™ StudyDegenerative Disc DiseaseScoliosis
NCT02657421Medtronic Spinal and Biologics168
Completed
Phase 2
Performance and Safety of Bone Substitute MBCP-FS in Maxillary Sinus Lift ProceduresSinus Implant Reconstruction
NCT00163605Baxter Healthcare Corporation86
Recruiting
Not Applicable
Study Protocol to Evaluate Clinical and Imaging Results of Knee Fresh Osteochondral AllograftsOsteochondral Defect
NCT04236492Fundació Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau40
Completed
Not Applicable
Observational Study of Clinical Performance of a Sterile, Bacteria-binding, Super-absorbent Wound DressingWounds
NCT02662218BSN Medical GmbH32