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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT03975101
Other study ID # VSEL-knee
Secondary ID
Status Withdrawn
Phase Phase 1/Phase 2
First received
Last updated
Start date July 5, 2019
Est. completion date June 15, 2020

Study information

Verified date May 2020
Source Fuda Cancer Hospital, Guangzhou
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of this study is the safety and efficacy of autologous very small embryonic-like stem cells(VSELs) to knee osteoarthritis.


Description:

VSELs come from the patient's peripheral blood, and will be injected in the most painful knee, or the worse knee on physical examination. Then follow-up the knee pain and imaging changes at 6 months and 1 year after treatment.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date June 15, 2020
Est. primary completion date May 25, 2020
Accepts healthy volunteers No
Gender All
Age group 50 Years to 60 Years
Eligibility Inclusion Criteria: - Patients had moderate to severe osteoarthritis of both knees. - Those had mechanical pain of knee joints, which was aggravated by walking or stair climbing. - Those complained of gelling pain of knee joint. - Those have crepitus and limitation of the joint range of motion with joint bony hypertrophy on physical examination, X-rays showed narrowing of joint space and osteophyte formation Exclusion Criteria: - Diabetic foot and patients with obvious edema in the legs caused by various causes - Blood disease patients, thrombocytopenia or dysfunction, hypofibrinemia or anticoagulant therapy, long-term use of aspirin

Study Design


Related Conditions & MeSH terms


Intervention

Biological:
very small embryonic-like stem cell
Mononuclear cells were collected from peripheral blood of each patient using a machine, VSELs were isolated, and each group was injected according to different numbers after activation

Locations

Country Name City State
China Biological treatment center in Fuda cancer hospital Guangzhou Guangdong

Sponsors (2)

Lead Sponsor Collaborator
Fuda Cancer Hospital, Guangzhou Guangzhou Four-Leaf Clover HealthTech Co., Ltd.

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change of knee pain score Pain assessment by visual analogue score (VAS). 0 point: no pain; 1-3 points: there is a slight pain that can be tolerated; 4-6 points: the patient has pain and affects sleep, and can still bear it; 7-10 points: the patient has progressively strong pain, pain is unbearable, affecting appetite and sleep 2-4 weeks after injection
Secondary Change of knee pain score Pain assessment by visual analogue score (VAS). 0 point: no pain; 1-3 points: there is a slight pain that can be tolerated; 4-6 points: the patient has pain and affects sleep, and can still bear it; 7-10 points: the patient has progressively strong pain, pain is unbearable, affecting appetite and sleep 6 months after injection
Secondary Imaging changes in the knee joint Magnetic resonance image (MRI) examination of the smoothness of the knee joint surface, ligament, soft tissue and meniscus damage 6 months after injection
Secondary Change of knee pain score Pain assessment by visual analogue score (VAS). 0 point: no pain; 1-3 points: there is a slight pain that can be tolerated; 4-6 points: the patient has pain and affects sleep, and can still bear it; 7-10 points: the patient has progressively strong pain, pain is unbearable, affecting appetite and sleep 12 months after injection
Secondary Imaging changes in the knee joint MRI examination of the smoothness of the knee joint surface, ligament, soft tissue and meniscus damage 12 months after injection
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