Cervicobrachial Neuralgia Clinical Trial
Official title:
Hypoalgesic Effect of Neural Mobilization in Cervicobrachial Pain Compared to a Controlled Group
Verified date | October 2019 |
Source | Universidad Europea de Madrid |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The purpose of these study is to compare the effectivity of the Cervical Lateral Glide physical therapy neural mobilization technique to the complete absence of treatment in a group of patients who suffer cervicobrachial pain.
Status | Completed |
Enrollment | 52 |
Est. completion date | October 2015 |
Est. primary completion date | October 2015 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 45 Years |
Eligibility |
Inclusion Criteria: - Clinical diagnosis of cervicobrachial pain confirmed by magnetic resonance imaging - Presence of unilateral symptoms of arm pain, paresthesia or numbness in the upper extremity during at least 3 continuous months previous to the application of treatment. - Positive results in all of the following tests: Spurling, Distraction, and Upper Limb Exclusion Criteria: - Contraindication in the use of nonsteroidal anti inflammatory drugs (NSAIDs) - The use of any type of treatment, therapy, procedure or drug to relieve pain - Patients who are under anticonvulsant, antidepressant or psychotropic medication - Vertebral instability - Vertebral osteoporosis - Vertebral or spine infection. - Neurologic diseases of genetic, infectious or neoplastic origin - Cervical stenosis myelopathy - Pregnancy - Kinesiophobia - Endocrine disorders and menopause - History of spine surgery - Intellectual disability, severe mental illness, intoxication, severe sleep deprivation, Alzheimer's disease. |
Country | Name | City | State |
---|---|---|---|
Venezuela | "Centro Médico y de Especialidades Pediátricas Dr. José Gregorio Hernández " | San Diego | Carabobo |
Lead Sponsor | Collaborator |
---|---|
Universidad Europea de Madrid |
Venezuela,
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* Note: There are 109 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change from baseline using the Numeric Rating Scale for Pain at 1 hour | the Numeric Rating scale for Pain (NRS) is an 11 point scale for patient self reporting of pain in which 0 points represents the total absence of pain and 10 points the worst state of pain, it was employed to evaluate the presence and relieve of cervicobrachial pain symptoms. | at baseline for both arms and 1 hour after the application of treatment only in the experimental arm, corresponding to intervention days 1, 15 and 30 | |
Secondary | Change from baseline of the Physical function involving the affected upper limb using the Quik DASH Scale | The disabilities of the arm quick test (Quick DASH) is a self report short questionnaire designed to measure physical function and symptoms in people with any or several musculoskeletal disorders of the upper limb. | at baseline, corresponding to intervention days 1 and 30 of treatment | |
Secondary | Cervical Rotation Range of Motion (CROM) | Cervical rotation was assessed in units of rotation degrees, using the cervical range-of-motion device (CROM). | at baseline for both arms and 1 hour after the application of treatment only in the experimental arm, corresponding to intervention days 1 and 30 |
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