lumbar discogenic pain.
Conditions
Interventions
Intervention 1: Intervention group: After the test description and written consent from the patient, about 20 cc of blood on ACD anticoagulant will be taken from the patient and immediately transferre
Sponsors
Kerman University of Medical Sciences
Eligibility
Sex/Gender
All
Age
20 Years to 60 Years
Inclusion criteria
Inclusion criteria: Patients aged between 20 and 60 years Patients with chronic low back pain caused by discopathy for more than 6 months Failure in commonly used medical treatments Damaged disc, annular rupture, or disc removed on radiograph The patient disk should be one level.
Exclusion criteria
Exclusion criteria: Existence of bleeding disorder Pregnancy Local or systemic infection Existence of a medical or psychological condition Narcotics Use
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain. Timepoint: 1 day, 1 week, 1 month, 6 months, 12 months, 18 months and 24 months after intervention. Method of measurement: Visual Analog Scale. | — |
Secondary
| Measure | Time frame |
|---|---|
| Disc changes on MRI. Timepoint: Three months before surgery,12 months and 24 months after intervention. Method of measurement: Pfirrmann scoring system. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactVahid Tavakolian ferdousie
Kerman University of Medical Sciences
Outcome results
None listed