Platelet-rich Plasma Clinical Trial
Official title:
Intradiscal Injection of Platelet-rich Plasma for Discogenic Pain in L-spine
Verified date | September 2019 |
Source | Show Chwan Memorial Hospital |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This study aims to evaluate the effect of platelet-rich plasma (PRP) on discogenic low back pain by comparing the pre- and post-interventional outcomes in patients receiving intradiscal injection of autologous PRP.
Status | Completed |
Enrollment | 30 |
Est. completion date | March 25, 2019 |
Est. primary completion date | March 25, 2019 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 20 Years to 60 Years |
Eligibility |
Inclusion Criteria: - Age between 20 and 60 years - L-spine disc degeneration diagnosed by MRI - Low back pain Exclusion Criteria: - Herniated disc - With prior history of spine surgery - With current or prior history of cancer - With current or prior history of hematological disease - Pregnancy - Patients who will not cooperate with one-year followup |
Country | Name | City | State |
---|---|---|---|
Taiwan | Show Chwan Memorial Hospital | Changhua City | Changhua |
Lead Sponsor | Collaborator |
---|---|
Pei-Yuan Lee, MD | Aeon Biotechnology Corporation |
Taiwan,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | 1-month postoperative function evaluated by Oswestry Disability Index | Function is evaluated using Oswestry Disability Index. | 1-month postoperative | |
Secondary | 4-month postoperative function evaluated by Oswestry Disability Index | Function is evaluated using Oswestry Disability Index | 4-month postoperative | |
Secondary | 1-month postoperative pain evaluated by visual analogue scale | Pain is evaluated using visual analogue scale | 1-month postoperative | |
Secondary | 4-month postoperative pain evaluated by visual analogue scale | Pain is evaluated using visual analogue scale | 4-month postoperative |
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