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Autologous Platelet Rich Plasma on Low Back Pain

Unknown statusNot applicableNCT02983747
View the official record on ClinicalTrials.gov

Recruiting status changes often. Contact the study team listed on ClinicalTrials.gov, and talk to your doctor before joining a study.

This study has no listed site in Canada in this snapshot. It is included as part of the worldwide chronic pain corpus.

Brief summary (from the registry)

The purpose of this study is to evaluate the effectiveness of autologous platelet-rich plasma (PRP) injection therapy for low back pain patients. Our hypothesis is that PRP will reduce the pain feeling and benefit for restore of the intervertebral disk.

Study details

Official title
Autologous Platelet Rich Plasma in Ultrasound Guided Intervertebral Disk Injection Therapy for Chronic Low Back Pain
Conditions
Interventions
  • Other: PRP Treatment(P)
  • Drug: Medication Treatment(Loxoprofen Sodium tablets,M)
Sponsor
Shanghai Changzheng Hospital
Start date
2019-11-01
Primary completion
2022-12-30
Sex
Male
Age range
from 18 Years to 45 Years
Results posted
No results posted in this snapshot
Countries
China
Total sites listed
1

Eligibility criteria

Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: * Chronic low back pain more than 2months * Visual analog scale score more than 4 * Positive X-ray, MRI or CT scan findings * Pfirrmann grading I-III * Well understanding and communication ability Exclusion Criteria: * History of allergy * Hemorrhagic trend or use of anticoagulant therapy * Mental diseases * Active infection or recent infectious diseases within 3 months * Local skin infection near the puncture location * Severe lumbar spinal stenosis, lumbar spondylolisthesis, ossification of posterior longitudinal * Ligament and lumbar disc herniation(more than 5mm) * Immunologic diseases * Tumors * Metastatic disease * Recent surgery less than 3 months) * Pregnancy

Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT02983747