Mechanical LBP(without radiculopathy). Lumbosacral plexus disorders
Conditions
Interventions
Intervention 1: Intervention group: For a period of one month, the lasers are powered by a 808nm diode laser device with a power supply of 160 mW, and the lumbar, trigger points, thunder points, and s
Treatment - Other
Treatment - Drugs
Intervention group: For a period of one month, the lasers are powered by a 808nm diode laser device with a power supply of 160 mW, and the lumbar, trigger points, thunder points, and some acupuncture
Control group: One month is used in the laser. Naproxen is given at a dose of 1000-250 mg daily for free (ie, if necessary) intake and daily intake is recorded in a table
Sponsors
Vice chancellor for research,Shahid Beheshti University of Medical Sciences
Eligibility
Sex/Gender
All
Age
20 Years to 70 Years
Inclusion criteria
Inclusion criteria: Inclusion criteria: Being over the age of; A written consent form has been signed; VAS level is between 10-3; According to the expert's diagnosis, the cause of their lower back pain is mechanical and lack of radiculopathy; Their lower back pain is more than three months; Exclusion criteria: Patients requiring emergency surgery:Bladder symptoms such as bladder loss, bladder loss, incontinence, lack of Sense while passing urine, Stomach incontinence , Anesthetizing around the anus ; Pregnancy; Discontinuation of the drug prescribed in / out of the protocol for the administration of the drug; A history of serious gastrointestinal complications (perforation / bleeding) due to the use of various types of NSAIDs; Being / detecting any type of cancer 6 patients with heart problems; Patients who have spinal cord stenosis;Radiculopathy (Pulmonary to subcutaneous pain); Sensory impairment; Muscle weakness; Patients who have taken rococtane over the past 3 months; Patients with asthma, allergic to aspirin or nasal polyps; Patients with severe depression and not being treated; Patients with psychosis;
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The degree of disability patients. Timepoint: One month after the treatment and the end of the third month. Method of measurement: Ronald-Morris Questionnaire and Oswestry Standard. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactDr.Leila Kholoosi
Laser Application Research Center in Medical Science
Outcome results
None listed