Radiculitis Clinical Trial
Official title:
Effectiveness of Neural Mobilization Techniques Compared to Standard Care Treatment in Patients With Lumbar Radiculitis: A Randomized Clinical Trial
The purpose of this study is to determine the effectiveness of neural mobilization techniques compared to standard care treatment in patients with lumbar radiculitis.
| Status | Not yet recruiting |
| Enrollment | 130 |
| Est. completion date | March 2020 |
| Est. primary completion date | March 2020 |
| Accepts healthy volunteers | No |
| Gender | All |
| Age group | 18 Years to 75 Years |
| Eligibility |
Inclusion Criteria: - Patients with low back pain and pain that radiates in the lower limb - Duration of symptoms > 6 weeks - Patients willing to be reassessed after 6 months - Patients willing to give written informed consent Exclusion Criteria: - History of spinal surgery - History of surgery or injury in the lower limbs in the past 6 months - Signs and symptoms of central nervous system involvement - Nerve root blocks for the past 6 weeks - History of diabetes - History of polyneuropathies - History of vascular pathologies in the lower limbs - History of systemic pathologies - History of inflammatory arthropathies |
| Country | Name | City | State |
|---|---|---|---|
| n/a | |||
| Lead Sponsor | Collaborator |
|---|---|
| Michalis Efstathiou |
Schäfer A, Hall T, Müller G, Briffa K. Outcomes differ between subgroups of patients with low back and leg pain following neural manual therapy: a prospective cohort study. Eur Spine J. 2011 Mar;20(3):482-90. doi: 10.1007/s00586-010-1632-2. Epub 2010 Dec — View Citation
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Visual Analogue Scale (VAS) - Measure assessing change | The VAS is a 100-point pain assessment scale ranging from 0 (no pain) to 100 (worst pain possible). | Change from baseline after 5 weeks and at 6 months | |
| Secondary | Roland Morris Disability Questionnaire (RMDQ) - Measure assessing change | The questioner measures the level of patients' disability. | Change from baseline after 5 weeks and at 6 months | |
| Secondary | Fear Avoidance and Beliefs Questionnaire (FABQ) - Measure assessing change | The questioner evaluates fear-avoidance beliefs of patients with low back pain in the clinical setting. | Change from baseline after 5 weeks and at 6 months | |
| Secondary | Handheld dynamometer - Measure assessing change | Changes in Muscle Strength assessed with the handheld dynamometer | Change from baseline after 5 weeks and at 6 months |
| Status | Clinical Trial | Phase | |
|---|---|---|---|
| Completed |
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