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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04089293
Other study ID # 7461
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date September 1, 2019
Est. completion date December 2019

Study information

Verified date July 2019
Source University Hospital, Strasbourg, France
Contact Philippe CLAVERT, MD, PhD
Phone 03 68 76 51 78
Email philippe.clavert@chru-strasbourg.fr
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The possibility of physiological contact between the deep surface of the tendon of the supraspinatus muscle and the labrum and/or posterior superior glenoidal rim during an armed movement of the arm (abduction and external rotation or ABER position) has been described for many years. The physiological hypotheses put forward to explain this contact are first of all that the intrinsic mobility of the scapulohumeral joint is limited by these 2 structures, that an anterior instability or micro-instability induces an abnormal anterior translation when performing an abduction and lateral rotation movement, or finally that there is a decrease in humeral retroversion. When this contact becomes symptomatic, it is called a posterior superior conflict. This pathology is mainly found in throwing athletes or athletes repeating maximum external rotation in the abducted position of the arm. This conflict is also described among some manual workers, and is then observed in an older age group.


Recruitment information / eligibility

Status Recruiting
Enrollment 100
Est. completion date December 2019
Est. primary completion date December 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion criteria:

- Major subject ((=18 years old)

- Operated subject (at the HUS between 01/01/2012 and 31/12/2013) under arthroscopy of anterior instability, of an unruptured tendinopathy of the rotator cuff, or of an extra-articular pathology.

- Subject not expressing opposition to the use of his data for research purposes

Exclusion criteria:

- Subject having expressed his opposition to participating in the study

- Patient under safeguard of justice

- Subject under guardianship or curatorship

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
France Service de chirurgie du membre supérieur Hautepierre 2 Strasbourg

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Strasbourg, France

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Study of posterior-superior contact in a patient with no rotator cuff lesion. The period from January 1st, 2012 to December 31st, 2013 will be examined
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