Clinical and Radiographic Outcomes in Arthroscopic "Inlay"Bristow Surgery With Screw Fixation vs Suture-button Fixation

NCT ID: NCT04460118

Last Updated: 2020-07-07

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

COMPLETED

Total Enrollment

117 participants

Study Classification

OBSERVATIONAL

Study Start Date

2018-09-01

Study Completion Date

2020-04-01

Brief Summary

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Retrospective comparative case-cohort study to investigate the efficacy of the modified arthroscopic Bristow-Latarjet surgery and to compare the clinical and radiographic outcomes using screw fixation vs suture-button fixation.

Detailed Description

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Background:Some studies have advocated the use of suture-button fixation during Bristow-latarjet surgery to reduce complications associated with screw fixation. However, these studies are not comparative studies, and their data are relatively incomplete.

Purpose: To compare the clinical and radiographic outcomes using screw fixation vs suture-button fixation.

Study Design: Retrospective comparative case-cohort study Methods: Patients who underwent the modified arthroscopic Bristow-Latarjet surgery between June 2015 and February 2018 were selected. Shoulders were separated into two groups based on surgical fixation method. Radiological results on 3D CT scan and clinical results were assessed preoperatively, immediately after operation, and postoperatively at 3 months, 6 months, 1 year and during the final follow-up.

Conditions

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Shoulder; Dislocation, Chronic

Study Design

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Observational Model Type

COHORT

Study Time Perspective

RETROSPECTIVE

Study Groups

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screw group

coracoid bone block fixed by the screw

Bristow surgery fixed by the screw

Intervention Type PROCEDURE

Bristow surgery fixed by the screw

button group

coracoid bone block fixed by the suture-button

Bristow surgery fixed by the suture button

Intervention Type PROCEDURE

Bristow surgery fixed by the suture button

Interventions

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Bristow surgery fixed by the screw

Bristow surgery fixed by the screw

Intervention Type PROCEDURE

Bristow surgery fixed by the suture button

Bristow surgery fixed by the suture button

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

1. a glenoid defect ≥10%
2. contact sport athletes with a glenoid defect \< 10%
3. failure after Bankart repair.

Exclusion Criteria

1. epilepsy
2. multidirectional shoulder instability
3. concomitant other lesions including rotator cuff tear, symptomatic acromioclavicular joint pathology or pathological involvement of the long head of the biceps
4. Follow-up was less than 2 years or incomplete follow-up data.
Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Peking University Third Hospital

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Guoqing Cui, professor

Role: PRINCIPAL_INVESTIGATOR

Peking University Third Hospital

Locations

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PekingUTH

Beijing, Beijing Municipality, China

Site Status

Countries

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China

Other Identifiers

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cui1

Identifier Type: -

Identifier Source: org_study_id

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