Comparative Study of Postieror Ankle Fracture

NCT ID: NCT03064386

Last Updated: 2017-02-27

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

50 participants

Study Classification

INTERVENTIONAL

Study Start Date

2017-02-28

Study Completion Date

2020-02-28

Brief Summary

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

To compare the clinical efficacy of open reduction and internal fixation (ORIF) with plate and screw for postieror malleolar fractures.

Detailed Description

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

Conditions

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

Postieror Malleolar Fracture Treatment

Study Design

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

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Participants Outcome Assessors

Study Groups

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

plate group

internal fixation with the plate

Group Type EXPERIMENTAL

Plate fixation

Intervention Type PROCEDURE

internal fixation with the plate

screw group

internal fixation with the screw

Group Type EXPERIMENTAL

Screw fixation

Intervention Type PROCEDURE

internal fixation with the screw

Interventions

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

Plate fixation

internal fixation with the plate

Intervention Type PROCEDURE

Screw fixation

internal fixation with the screw

Intervention Type PROCEDURE

Eligibility Criteria

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

Inclusion Criteria

supination-external rotation Ⅳ type injury

Exclusion Criteria

Pion fracture; Isolated posterior ankle fracture.
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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

Shanghai Tongji Hospital, Tongji University School of Medicine

OTHER

Sponsor Role lead

Responsible Party

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

Liming Cheng

Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Central Contacts

Reach out to these primary contacts for questions about participation or study logistics.

Yunfeng Yang, Ph.D.

Role: CONTACT

+86 13918588939

Other Identifiers

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

56014768-6

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

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

Surgery of the Pilon Fractures
NCT03367169 TERMINATED NA