Could a simple blood injection ease your back pain?
NCT ID NCT03712527
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tested whether a single injection of platelet-rich plasma (PRP) into the spinal disc could reduce pain and improve function in people with chronic low back pain caused by active discopathy. 126 adults aged 18 to 60 with at least 3 months of pain received either PRP or a placebo (saline) injection. The main goal was to see if at least 30% more people in the PRP group reported meaningful improvement after 3 months.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- platelet-rich plasma (PRP)
- What this could lead to
- If it works, this could offer a new, non-surgical option to ease pain and improve function for people with chronic low back pain from active discopathy.
- What could go wrong
- This is a small, early-stage trial with only 126 participants. The treatment may not work better than a placebo, and results may not apply to everyone with back pain.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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126 people
The number who actually took part.
- Started
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Nov 2018
- Finished
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Feb 2026
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 60 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * \- Age between 18 to 60 years * Patient with AD characterized by a common lumbar spine for more than 3 months associated with Modic I discopathy on MRI on a single level * Annulus fibrosus capable of holding the cell implantation, demonstrated by MRI (stages \< 5 of Pfirrmann's score). The Pfirrmann's score is fully described in annex (Pfirrmann et al. 2001). * Daily LBP for at least 3 month with baseline mean intensity ≥ 40 mm on VAS (0-100) in the previous 48 hours * Written and signed informed consent form * Subjects must be covered by public health insurance * Subjects must be able to attend all scheduled visits and to comply with all trial procedures Exclusion Criteria: * \- Patient with Modic 1 discopathy in different vertebral levels * Patient with a Modic I signal abnormality related to a static spinal disorder (such as previous vertebral fractures, or isthmic lysis, or spondyloarthritis) * Patient with a history of lumbar spine surgery * Patient with suspected spondylodiscitis or other infection * Patient under anticoagulant or antiaggregant therapy, or with a coagulation disorder * Patient with allergy to iodine or to any of the components of Xylocaine * Contraindication to MRI: Pacemaker or neurosensorial stimulator or implantable defibrillator, cochlear implant, ferromagnetic foreign body similar to the nervous structure. * Patient with anatomical difficulty of access to the injection area (judged by the investigator) * Patient with an uncontrolled severe disease (i.e. heart, pulmonary, gastro-intestinal, neurologic, endocrine, auto-immune affections) limiting the patient's safety (judged by the investigator) * Patient with previous malignancy less than 5 years (except for non-melanoma skin cancer) * Prior to the screening visit: * a current and recent use of morphine (\< 1 month) * a systemic or local corticosteroid therapy (\< 1 month) * Porphyria * Patient with sphincter disorders indicating a cauda equina syndrome * Psychotic state not controlled by a treatment * Pregnancy (βHCG positive), breast-feeding or the absence of effective contraception for women of child-bearing age * Vulnerable persons protected by law * Persons under guardianship * Subject who are in a dependency or employment with the sponsor or the investigator * Participation in another clinical trial * Subject unable to read or/and write
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Genom att skicka in godkänner du våra Användarvillkor
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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APHP Cochin
Paris, France
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CHU Bordeaux
Bordeaux, France
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CHU Nice
Nice, France
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CHU Nîmes
Nîmes, France
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CHU Toulouse
Toulouse, France
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Univesity Hospital od Montpellier
Montpellier, 34295, France
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