Patients with pain complaints as a result of lumbar foraminal stenosis Musculoskeletal Diseases
Conditions
Interventions
The project involves the administration of a single dose of a hybrid form of hyaluronic acid called Sinovial HL, under ultrasound guidance, in the zone of expected compression of the nerve root from t
Sponsors
Sutherland Medical Center
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1. Clinical symptoms of radicular pain in the lumbar region 2. MRI confirmed recital stenosis of degenerative origin 3. No other spine diseases (post-traumatic, systemic inflammatory diseases, cancer, birth defects) 4. Adults consenting to the injection 5. Mental contact ensuring cooperation in the period of neuromobilization
Exclusion criteria
Exclusion criteria: 1. Neurological deficit 2. The presence of other spine diseases (post-traumatic, systemic inflammatory diseases, neoplasms, birth defects) 3. Refusal to consent to the injection 4. Anticoagulants, other injection contraindications 5. Impeded contact with the patient, not promising cooperation during the period of neuromobilization
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1. Pain assessed using the Numerical Rating Scale (NRS, 1-10) at baseline and 1, 2, and 3 months after the intervention 2. Pain assessed using the Roland – Morris scale at baseline and 1, 2, and 3 months after the intervention 3. Pain assessed using the Straight Leg Raise Test (SLR test) at baseline and 1, 2, and 3 months after the intervention | — |
Secondary
| Measure | Time frame |
|---|---|
| Disability assessed using the Oswestry Low Back Pain Disability Questionnaire at baseline and 1, 2, and 3 months after the intervention | — |
Countries
Poland
Outcome results
None listed