Transitional Ankle Fracture Management Using a New Joystick Technique

NCT ID: NCT05012449

Last Updated: 2021-08-19

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

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Recruitment Status

ACTIVE_NOT_RECRUITING

Clinical Phase

NA

Total Enrollment

30 participants

Study Classification

INTERVENTIONAL

Study Start Date

2021-07-01

Study Completion Date

2025-12-31

Brief Summary

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To investigate the feasibility and short-term clinical efficacy of the arthrography-assisted joystick technique for the treatment of adolescent transitional ankle fracture.

Detailed Description

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Adolescent transitional ankle fracture who were treated with the arthrography-assisted joystick technology.

Conditions

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Tibial Fracture

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

CROSSOVER

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Arthrography-assisted joystick technology.

Adolescent transitional ankle fracture who were treated with the arthrography-assisted joystick technology.

Group Type EXPERIMENTAL

Arthrography-assisted joystick technology.

Intervention Type PROCEDURE

Arthrography-assisted joystick technology.

No arthrography-assisted joystick technology.

Adolescent transitional ankle fracture who were treated with open or close reduction .

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Arthrography-assisted joystick technology.

Arthrography-assisted joystick technology.

Intervention Type PROCEDURE

Other Intervention Names

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No arthrography-assisted joystick technology.

Eligibility Criteria

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Inclusion Criteria

1. X-ray or computed tomography (CT) diagnosis of adolescent transitional ankle fracture.
2. After manual reduction, the displacement of both ends of the epiphyseal plate or articular surface fracture in any direction was still \> 2 mm; the arthrography-assisted joystick technique was used for treatment.

Exclusion Criteria

1. Bilateral fracture.
2. In association with epiphyseal dysplasia and neuromuscular disease.
Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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The Fuzhou No 2 Hospital

OTHER

Sponsor Role lead

Responsible Party

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Shunyou Chen

Clinical Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Shunyou Chen, doctor

Role: STUDY_CHAIR

The Fuzhou No 2 Hospital

Locations

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Shunyou Chen

Fuzhou, Fujian, China

Site Status

Countries

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China

Other Identifiers

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Shunyou

Identifier Type: -

Identifier Source: org_study_id

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