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Dynamic Humeral Centering in Impingement Syndrome

NCT ID: NCT01022775

Last Updated: 2009-12-01

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

Clinical Phase

PHASE3

Total Enrollment

70 participants

Study Classification

INTERVENTIONAL

Study Start Date

2001-04-30

Study Completion Date

2007-02-28

Brief Summary

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The purpose of this study is to determine wether dynamic humeral centering is effective in patients with impingement syndrome of the shoulder

Detailed Description

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Clinical trial with randomization for treatment and physiotherapist

Conditions

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Degenerative Rotator Cuff Disease With Impingement Syndrome

Keywords

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Degenerative rotator cuff disease Impingement syndrome Dynamic humeral centering Randomized clinical trial

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Outcome Assessors

Study Groups

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1: Dynamic humeral centering

Dynamic humeral centering performed for 6 weeks, in 15 supervised individual outpatient sessions, plus daily home exercises for 12 months.

Group Type EXPERIMENTAL

Dynamic humeral centering

Intervention Type PROCEDURE

Dynamic humeral centering performed for 6 weeks, in 15 supervised individual outpatient sessions, plus daily home exercises for 12 months.

2: Nonspecific mobilisation

Nonspecific mobilisation performed for 6 weeks, in 15 supervised individual outpatient sessions, plus daily home exercises for 12 months.

Group Type ACTIVE_COMPARATOR

Nonspecific mobilisation

Intervention Type PROCEDURE

Nonspecific mobilisation performed for 6 weeks, in 15 supervised individual outpatient sessions, plus daily home exercises for 12 months.

Interventions

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Dynamic humeral centering

Dynamic humeral centering performed for 6 weeks, in 15 supervised individual outpatient sessions, plus daily home exercises for 12 months.

Intervention Type PROCEDURE

Nonspecific mobilisation

Nonspecific mobilisation performed for 6 weeks, in 15 supervised individual outpatient sessions, plus daily home exercises for 12 months.

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* age \> 30 years
* pain duration \> 1 month
* presence of at least 2 positive impingement test results from Neer, Yocum and Hawkins testing
* total Constant score \< 80.

Exclusion Criteria

* stiffness
* anteroposterior instability
* tendinous calcification
* corticosteroid injection within the previous 30 days
* previous surgery
* humeral fracture
* inflammatory joint disease
* neoplastic disorders
Minimum Eligible Age

31 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Societe Francaise de Rhumatologie

OTHER

Sponsor Role collaborator

Assistance Publique - Hôpitaux de Paris

OTHER

Sponsor Role lead

Responsible Party

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Department of clinical research and development

Principal Investigators

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Johann BEAUDREUIL, MD,PhD

Role: PRINCIPAL_INVESTIGATOR

Assistance Publique - Hôpitaux de Paris

Locations

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Department of Rheumatology, Lariboisière Hospital

Paris, , France

Site Status

Countries

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France

References

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Beaudreuil J, Ostertag A, Lasbleiz S, Vicaut E, Yelnik A, Bardin T, Orcel P. Efficacy of dynamic humeral centering according to Neer test results: a stratified analysis of a randomized-controlled trial. Int J Rehabil Res. 2015 Mar;38(1):81-3. doi: 10.1097/MRR.0000000000000079.

Reference Type DERIVED
PMID: 25185788 (View on PubMed)

Beaudreuil J, Lasbleiz S, Richette P, Seguin G, Rastel C, Aout M, Vicaut E, Cohen-Solal M, Liote F, de Vernejoul MC, Bardin T, Orcel P. Assessment of dynamic humeral centering in shoulder pain with impingement syndrome: a randomised clinical trial. Ann Rheum Dis. 2011 Sep;70(9):1613-8. doi: 10.1136/ard.2010.147694. Epub 2011 May 29.

Reference Type DERIVED
PMID: 21623001 (View on PubMed)

Other Identifiers

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CRC99241

Identifier Type: OTHER

Identifier Source: secondary_id

P000203

Identifier Type: -

Identifier Source: org_study_id