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A Comparative Study: Non-Surgical Spinal Decompression and Spinal Manipulative Therapy- Utilizing a Quantifiable Musculoskeletal Functional Assessment Risk Analysis Tool (MSDR®) in Patients With Chronic Low Back Pain

M

MedAppraise

Status

Unknown

Conditions

Chronic Low Back Pain

Treatments

Other: MSDR

Study type

Interventional

Funder types

Industry

Identifiers

NCT00732394
TCT06-002

Details and patient eligibility

About

To administer the MSDR® (Musculoskeletal Disorder Reporting) instrument to document the musculoskeletal profile of patients with chronic low back pain, a prospective, non-randomized, multicenter treatment trial

Enrollment

200 estimated patients

Sex

All

Ages

18 to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Must have Informed Consent Signed
  • Lumbar Disc Herniations under 5mm without Sequestered Fragments
  • Lumbar Disc Bulging
  • Lumbar Degenerative Disc Disease (mild and moderate severity)
  • Non-pregnant Females and Males suffering from Chronic Low Back Pain from 18 to 65 years of age
  • Segmental Dysfunction Secondary to Dyskinesia
  • Unresolved Nerve Entrapment Syndrome
  • Patients must be able to comply with study protocol
  • Joint Fixation Syndrome
  • Premenopausal Female Patients, excluding patients who have undergone a hysterectomy, oophorectomy, or tubal ligation, must have one of the following methods of contraception and must have a negative serum or urine b-HCG pregnancy test performed within 48 hours before initiating protocol specified treatment.

Exclusion criteria

  • Contraindications to Spinal Manipulative Therapy

  • Lumbar Canal Stenosis resulting in significant neurological comprimise

  • Any Spinal Cord Compression resulting in significant neurological comprimise

  • Cauda Equina Syndrome

  • Infection

  • Osteomyelitis

    ->65 years of age

  • History of Back or Neck Surgery

  • Acute Arthritis

  • Signs or Symptoms of Arterial Aneurysm

  • History of Active Cancer with Bone Metastasis

  • Widespread Staphyloccal and/or Strepococcal Infection

  • Acute Gout

  • Serious unstable medical illness such as cardiovascular, renal, respiratory, endocrine, gastrointestinal, or psychiatric.

  • Unstable Spondylosis, Spondylolisthesis, or Spondylolysis

  • Prior adverse experience with Spinal Manipulation Therapy

  • Uncontrolled Diabetic Neuropathy

  • Gonorreal Spinal Arthritis

  • Tuberculosis to the Bone

  • Maligancy with Metatasis to Bone

  • Excessive Spinal Osteoporosis

  • Osteomalacia

  • Ankylosis

  • Syphlitic Articular or Peri-Articular Lesions

  • Active Low Back Injury Resulting from a Motor Vehicle Accident or Work Related Injury

Trial design

Primary purpose

Screening

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

Trial contacts and locations

1

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Central trial contact

Eric K Groteke, DC; Damon J Stafford, DC

Data sourced from clinicaltrials.gov

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