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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT03331510
Other study ID # Prospective Strength Latarjet
Secondary ID
Status Not yet recruiting
Phase N/A
First received November 1, 2017
Last updated November 30, 2017
Start date February 2018
Est. completion date December 2022

Study information

Verified date November 2017
Source Etzel Clinic
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Open and arthroscopic Latarjet procedures are used to treat shoulder instability as primary and salvage procedures. During surgery the coracoid process is detached and repositioned to the anterior glenoid through a subscapularis split and fixed in place, resulting in an enlarged glenoid and therefor articular surface. However, before this is done, the pectorals minor, which inserts at the coracoid process, has to be detached and is left without further treatment. Moreover, the conjoint tendon, the origin of the short head of the biceps and coracobrachialis, is repositioned with the coracoid and therefor distalized and medialized.

No study currently followed up on the strength of the muscles altered. The aim of this study is therefor, to prospectively measure range of motion and strength of the operated shoulder at different time points pre- and postoperatively, comparing it with the healthy shoulder in each individual.


Description:

Strength, range of motion and stability will be assessed pre-operatively and at 6 weeks, 12 weeks, 6 months, 12 months and 24 months post-operatively. Next to standard radiological follow up, including X-ray, arthrographic computed tomography as well as arthrographic magnetic resonance imaging, specific shoulder scores will be utilised. Strength for general shoulder motion as well as specifically for the subscapularis, the pectorals minor, the coracobrachialis and the biceps will be measured with a shoulder dynamometer. Data will be analysed and published.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 50
Est. completion date December 2022
Est. primary completion date January 2022
Accepts healthy volunteers
Gender All
Age group 18 Years to 50 Years
Eligibility Inclusion Criteria:

- Patients who experienced at least one shoulder dislocation.

- Patients who are willing to participate in the study

- Patients who receive arthroscopic Latarjet procedure for treatment of glen-humeral instability

- Patients who are at least 18 years old.

- Patients with an ISI-Score of at least 4 points.

Exclusion Criteria:

- Patients older than 50 or younger than 18 years of age.

- Patients with painful unstable (multidirectional) instability

- Patients with congenital defects of the bones involved (humerus, scapula).

- Patients with an ISIS of smaller 4 points.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Strength testing before and after arthroscopic Latarjet
After patients, based on the ISI-Score, were assigned to treat their shoulder instability with an arthroscopic Latarjet procedure, they are eligible for this study. Strength of different involved muscles, as well as ROM will be measured before and at several time points after surgery.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Etzel Clinic

Outcome

Type Measure Description Time frame Safety issue
Primary Strength Strength for different muscles involved in shoulder movement is measured pre- and post-operatively for the operated shoulder and the contralateral side. Strength will be measured in Kilogramm with a shoulder dynamometer. Scale range is assumed to be between 0 and 25 kg, higher values postoperatively indicate better outcome. Measurements will be undertaken for the subscapularis in internal rotation at 0 and 90 degrees; for the muscles attached to the conjoint tendon (short head of the biceps and coracobrachialis) in 45 degree shoulder flexion, while resistance will be applied on the flexing forearm. The pectoralis minor measurment will be undertaken through applying pressure against the protracting shoulder. Furthermore, standard strength measurements will be undertaken in 90 degree shoulder flexion and abduction, applying resistance against the hand, and in 0 degree internal as well as external rotation with a flexed elbow. 24 months
Secondary Range of Motion Range of Motion of the operated shoulder and the contralateral side is measured pre-and post-operatively. Outcome measure will be in degree of range of motion, with higher numbers indicating greater range of motion. 24 months
Secondary Stability Stability of the operated shoulder is evaluated objectively and subjectively utilising different specific scores. 24 months
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