Ankle Arthrodesis Nail for 2-level Pathologic Tibial Fracture

NCT ID: NCT04940754

Last Updated: 2021-08-17

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

1 participants

Study Classification

INTERVENTIONAL

Study Start Date

2021-04-08

Study Completion Date

2022-05-08

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

Tibial pseudarthrosis in 83 year old patient suffering from pathologic fractures

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

The arthrodesis nail for hind foot problems is used as salvage for tibial fractures after failed plate fixation,

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Bone Metastases Fracture Nonunion Bone Lesion

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

NA

Intervention Model

SINGLE_GROUP

Use of an approved implant for expanded application
Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Stabilzation of Fracture

Arthrodesis nail used for stabilzation of a fracture, single patient

Group Type OTHER

osteosynthesis

Intervention Type PROCEDURE

Closed reduction, internal fixation

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

osteosynthesis

Closed reduction, internal fixation

Intervention Type PROCEDURE

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

\- old age, fragility fracture, tibia

Exclusion Criteria

* active osteomyelitis
Minimum Eligible Age

80 Years

Maximum Eligible Age

90 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Orthopaedie Zentrum Zuerich

NETWORK

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Responsibility Role SPONSOR

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Orthopaedie Zentrum Zuerich

Zurich, , Switzerland

Site Status

Countries

Review the countries where the study has at least one active or historical site.

Switzerland

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

GUE

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

Non Randomized Humerusshaft Fracture
NCT00205972 COMPLETED PHASE4