Chiropractic Prone Distraction for Lower Back Pain
Herniated Disc, Lower Back Pain, Sciatica
About this trial
This is an interventional treatment trial for Herniated Disc
Eligibility Criteria
Inclusion Criteria: Active Duty military personnel Aged 18-45 (age is limited to 45 years due to the natural aging and degeneration of the discs; the less hydration the disc maintain, the less likely manipulation will be successful). Have subacute low back pain (more than three months duration but less than six months duration), with radicular component (sciatica) rated at a minimum level of 4 on the Numerical Rating Scale (NRS) of the Brief Pain Inventory Have a confirmed herniated disc, as noted on MRI, which correlates with the clinical findings (sciatica) In this study, a "herniated disc" refers to any localized displacement of disc material, including nucleus, cartilage, fragmented apophyseal bone, or fragmented anular tissue, which results in back and leg pain. "Herniated Disc" also will include disc extrusions and disc bulges (protrusions) only when with associated annular tears. In this study, "sciatica" refers to pain in the lower extremity/ies that follows the course of the sciatic nerve Exclusion Criteria: Patients who are not able to give informed consent. Pregnant or nursing women Patients who have a primary bone disease, cancer, infection, spondylolysis or spondylolisthesis. Patients who have had prior spine surgery, including rhizotomy Participation in another conflicting research study Patients who cannot commit to a trial lasting up to eight weeks or cannot come for bi-weekly treatments Patients who are going through a course of physical therapy or chiropractic treatment or at the time of planned enrollment or are being currently being managed and/or treated for any pain condition Patients who have an unstable medical or psychiatric condition Patients who are planning or have been advised to have spine surgery Any contraindications to either prone distraction or side posture manipulation will disqualify potential subjects from any participation in this study Patients with a pacemaker.
Sites / Locations
- National Naval Medical Center