Status:

COMPLETED

Clinical Evaluation of the Effects of Mirror Therapy in Patients With Complex Regional Pain Syndrome (CRPS) Type 1

Lead Sponsor:

Ankara University

Conditions:

Complex Regional Pain Syndrome Type I

Eligibility:

All Genders

18-80 years

Phase:

NA

Brief Summary

CRPS Type 1 can occur after traumas, surgical applications or central nervous system disorders. The triggering factor in CRPS type 1 is fracture in about half of the cases. Mirror therapy is an innova...

Detailed Description

This study is planned as a prospective randomized single blind controlled study. It was approved by the Ankara University Faculty of Medicine Ethics Committee and was conducted in accordance with the ...

Eligibility Criteria

Inclusion

  • Adult individuals over 18 years of age
  • CRPS type 1 diagnosis according to 2003 Budapest diagnostic criteria
  • Patients who developed CRPS Type 1 due to traumatic causes (surgical procedures, fractures, immobilization)
  • Patients who agree to participate in the study and sign the informed consent form

Exclusion

  • Patients with peripheral nerve injuries (those with a diagnosis of CRPS type 2 according to Budapest criteria)
  • Patients with CRPS Type 1 after central nervous system injury (stroke)
  • Patients in the acute and post-acute rehabilitation who have had primary or secondary tendon repair of the hand
  • The presence of comorbid conditions (e.g. decompensated heart failure, chronic renal insufficiency, malignancy) that would impair the functioning of the person and the health-related quality of life
  • The presence of comorbid disease affecting hand function (e.g. rheumatoid arthritis, psoriatic arthritis or other inflammatory diseases that cause hand involvement)
  • Patients with acute deep venous thrombosis and arterial thrombosis of the upper extremity
  • Patients with arterial / venous injury and / or undergoing arterial revascularization
  • Patients with excessive alcohol and inappropriate opioid use
  • Patients with untreated psychiatric problems (major depression, anxiety, schizophrenia, etc.)
  • Patients with recurrent CRPS Type 1

Key Trial Info

Start Date :

March 1 2017

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

January 31 2020

Estimated Enrollment :

36 Patients enrolled

Trial Details

Trial ID

NCT03377504

Start Date

March 1 2017

End Date

January 31 2020

Last Update

February 25 2020

Active Locations (1)

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Ankara University Faculty of Medicine, İbn-i Sina Research and Application Hospital

Ankara, Turkey (Türkiye), 06030