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Profiling the RCRSP Patient: a Pain Phenotype Classification Algorithm

U

University of Thessaly

Status

Not yet enrolling

Conditions

Rotator Cuff Tear or Rupture, Not Specified as Traumatic
Rotator Cuff Impingement
Rotator Cuff Tendinosis
Rotator Cuff Syndrome
Rotator Cuff Tears

Treatments

Device: Quantitative Sensory Testing / Dynamometry / Goniometry

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

The aim of this study is to collect a sum of different characteristics that have been mentioned previously in people presenting with RCRSP and by clustering them to create a phenotype system which may assist the individualisation of their management

Full description

This study will be conducted at a hospital environment by recruiting people that will seek help for their shoulder pain by a specialist upper- limb Orthopaedic Surgeon at the Department of Hand & Upper Limb Microsurgery of the 'KAT General Hospital' in Athens, Greece. Participants that will be diagnosed with RCRSP by the orthopaedic surgeon and fulfil the eligibility criteria will undergo a series of one-off measurements. Written consent will have to be obtained before a sum of self-reported outcome measures and objective testing will take place. The main categories for which outcome measures will be used are: pain, function, psychosocial and lifestyle factors.

Enrollment

100 estimated patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age: 18-65
  • Pain: >3 months, non-traumatic, unilateral or bilateral of anterolateral location
  • ROM: >50% all planes, AROM painful in forward flexion and/or abduction
  • Provocation testing: Hawkins-Kennedy, Neer, Painful Arc, Resisted ER, Empty Can (3 or more out of the 5 +ve)

Exclusion criteria

  • Pain < 3months
  • History of neck or shoulder trauma
  • Radicular signs, shoulder pain reproduced with neck movements
  • GH OA
  • Frozen Shoulder
  • Tears >C3 according to Snyder Classification
  • Fibromyalgia
  • Neurological, systemic local or autoimmune inflammatory conditions
  • Clinical depression
  • No injected corticosteroids or physiotherapy the last 3/12

Trial contacts and locations

0

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Central trial contact

ACHILLEAS PALIOURAS, PT, MSc

Data sourced from clinicaltrials.gov

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