Clinical Study on Diagnostics and Outcome of Ruptures of the Subscapularis After Arthroscopic Refixation

NCT ID: NCT02383914

Last Updated: 2020-11-06

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

32 participants

Study Classification

OBSERVATIONAL

Study Start Date

2014-03-31

Study Completion Date

2018-10-31

Brief Summary

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The purpose of the trial is to optimize the diagnostics of subscapularis tendon tears and as the circumstances require to found a new classification.

The prime objective is a comparison of the conclusive of the clinic check-up, the sonographic and magnetic resonance tomography findings.

The secondary objective is to detect the correlation of the outcome with the age , the gender, the pathogenesis and attendant injuries.

Detailed Description

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Conditions

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Subscapularis Tendon Rupture

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Subscapularis rupture

No interventions assigned to this group

Eligibility Criteria

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Inclusion Criteria

* patients, who have turned 18
* suspected subscapularis tendon rupture

Exclusion Criteria

* disability to understand the trial
* intraoperative intact supbscapularis tendon
* pre-surgical operation of the affected shoulder
* tumor
* infection
Minimum Eligible Age

18 Years

Maximum Eligible Age

75 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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University of Rostock

OTHER

Sponsor Role lead

Responsible Party

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PD Dr. med. Thomas Tischer

Prof. Dr. med. Thomas Tischer

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Orthopaedic Clinic of the University of Rostock

Rostock, Mecklenburg-Vorpommern, Germany

Site Status

Countries

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Germany

Other Identifiers

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Subscap-042014

Identifier Type: -

Identifier Source: org_study_id