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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04960137
Other study ID # D2016052
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date September 1, 2017
Est. completion date February 28, 2019

Study information

Verified date July 2021
Source Peking University Third Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to conduct a comparative study through clinical trials to verify the safety and efficacy of the products in the experimental group for clinical use.


Description:

The product of this clinical validation is the fixed button plate system, which is used for the reconstruction of the coracoclavicular ligament in the treatment of recurrent shoulder dislocation. The clinical trial was conducted to verify the rationality of its structural design, the convenience of its operation, and the effectiveness and safety of its clinical use. This trial was conducted in a parallel controlled trial design, the patients were divided into test and control groups to evaluate the safety and efficacy of the product.


Recruitment information / eligibility

Status Completed
Enrollment 100
Est. completion date February 28, 2019
Est. primary completion date September 30, 2018
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility 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.

Study Design


Related Conditions & MeSH terms


Intervention

Device:
button plates fixation system
The button plates fixation system consists of fixing plate, prefabricated mix, button and fuse. In the process of use, the fuse plays the role of guiding the fixed plate through, pulling the button and shortening the distance between the button and the fixed plate. The prefabricated mix is pre-worn between the button and the fixed plate, and the lead pulls the distance between the fixed plate and the button after tightening and fixing. Prefabricated mix, make mix tight and knot. Finish the preliminary work of fixing.
Non-absorbable Suture Anchor
A conventional device used in surgery for shoulder dislocation.

Locations

Country Name City State
China PekingUTH Beijing Beijing

Sponsors (3)

Lead Sponsor Collaborator
Peking University Third Hospital Hunan People's Hospital, The First Hispital of Jilin University

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Rowe score The Rowe score is an internationally recognized scoring system for the assessment of shoulder function. before surgery
Primary Rowe score The Rowe score is an internationally recognized scoring system for the assessment of shoulder function. 3 months after surgery
Primary Rowe score The Rowe score is an internationally recognized scoring system for the assessment of shoulder function. 6 months after surgery
Secondary ASES score The American Shoulder and Elbow Surgeons (ASES) score is the most commonly used score to describe the function of patients' shoulder joints, ranging from 0 to 100. The higher the score, the better the function of patients' shoulder joints. before surgery
Secondary ASES score The American Shoulder and Elbow Surgeons (ASES) score is the most commonly used score to describe the function of patients' shoulder joints, ranging from 0 to 100. The higher the score, the better the function of patients' shoulder joints. 3 months after surgery
Secondary ASES score The American Shoulder and Elbow Surgeons (ASES) score is the most commonly used score to describe the function of patients' shoulder joints, ranging from 0 to 100. The higher the score, the better the function of patients' shoulder joints. 6 months after surgery
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