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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06109220
Other study ID # KY20232112-X-1
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date March 30, 2023
Est. completion date December 30, 2024

Study information

Verified date March 2023
Source Xijing Hospital
Contact Yanyan Jia
Phone +862984771794
Email xiyyllwyh@163.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study was to analyze and study the efficacy and safety of autologous adipose-derived vascular matrix components (SVF) in patients with knee osteoarthritis before and after treatment through clinical evaluation, radiation index, and metabolic index comparison between plasma and irrigation solution before and after SVF injection.


Recruitment information / eligibility

Status Recruiting
Enrollment 30
Est. completion date December 30, 2024
Est. primary completion date June 30, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 20 Years to 70 Years
Eligibility Inclusion Criteria: - The age range is 20-70 years old - Patients with unilateral or bilateral knee degenerative inflammation (KOA) with Kellgren-lawrence rating of level 3 or lower - The physical health status is mainly in the ASA grade ?, ? and ? - Subjects had no active tumors, no active inflammation, no treponema pallidum, HIV, hepatitis B virus, or hepatitis C virus - The subject shall provide the physical examination report of knee X-ray examination, MRI examination and other items Exclusion Criteria: - Patients with nonunion or displaced fractures around defective cartilage - Pregnant or lactating women - Autoimmune disease - Subjects with diabetes (exceptions are patients whose blood sugar levels remain within the normal range and diabetes has not caused other complications) - The patients had severe neurological diseases affecting the evaluation of postoperative results

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Stromal vascular fraction,SVF
SVF was injected into the knee cavity

Locations

Country Name City State
China Xijing Hospital Xi'an Shannxi

Sponsors (1)

Lead Sponsor Collaborator
Xijing Hospital

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary T2 mapping The degree of change of articular cartilage was observed 24 months after the first SVF injection into the knee cavity
Secondary Western Ontario and McMaster Universities Arthritis Index (WOMAC) The WOMAC is a specific assessment scale for osteoarthritis, which is assessed according to three aspects: pain, stiffness and function. A total of 24 WOMAC scores were scored, 0-10 points for each item, with a total score of 240 points. A total score <80 was mild OA, a total score of 80-120 was moderate OA, and a total score of >120 was severe OA.The severity and therapeutic effect of arthritis were evaluated according to the relevant symptoms and signs of patients. 24 months after the first SVF injection into the knee cavity
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