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Efficacy of PRP for bone fusion in LLIF

Phase 1
Conditions
vertebral fracture, lumbar canal stenosis, lumbar spondylolisthesis, adult spine deformity
Registration Number
JPRN-jRCTb032200199
Lead Sponsor
Yamazaki Masashi
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
15
Inclusion Criteria

1. Patients who receives lateral lumbar interbody fusion surgery for vertebral fracture, lumbar canal stenosis, lumbar spondylolisthesis, adult spine deformity, and so on
2. Patients who receives lateral lumbar interbody fusion surgery at 1-4 levels
3. Patients over 20 years old
4. Patients with informed concent and understanding for treatment

Exclusion Criteria

1. Patients with a history of lumbar surgery, purulent spondylitis, or spinal tumor
2. Patients who received other Investigational new drug within 3 months of participating in this clinical study
3. Patients who have a primary illness that is clearly inferior to bone formation (bone metabolic disease, dialysis, and so on)
4. Patients who have uncontrolled diabetes
5. Patients with anemia (Hb<9.0g/dL)
6. Patients who have disorder of blood coagulation.
7. Patients with rheumatoid arthritis who are using biologics with high risk of perioperative infection.
8. Women who are pregnant or suspected ofbeing pregnant or breastfeeding
9. Patients with metal allergy
10. Patients who needs the legal representative
11. Patients who are judged inappropriate by the responsible doctor for the study

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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