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Effect of platelet-rich plasma on discopathic pai

Not Applicable
Recruiting
Conditions
lumbar discogenic pain.
Registration Number
IRCT20210128050164N1
Lead Sponsor
Kerman University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
40
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

Existence of bleeding disorder
Pregnancy
Local or systemic infection
Existence of a medical or psychological condition
Narcotics Use

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
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 Outcome Measures
NameTimeMethod
Disc changes on MRI. Timepoint: Three months before surgery,12 months and 24 months after intervention. Method of measurement: Pfirrmann scoring system.
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