Important Note: Redirection of Services to ChiCTR
We would like to inform you that the Clinical Trial Registry page will discontinue the function of updating trial information directly on this platform. However, you will still be able to view the existing registration details. For any updates to trial information, you can use the China Clinical Trial Registry (ChiCTR) directly at https://www.chictr.org.cn. This change will be fully implemented by 2024-Aug-05. Thank you for your attention.
CUHK_CCT00469
2015-08-20
Prospective
2014.279-T
The Chinese University of Hong Kong
Prof. Kevin HO Ki Wai
Prof. G. Li
Form a group with the primary sponsor in which the responsibilities of sponsorship are allocated among the members of the group
Queena Poon
Department of Orthopaedics and Traumatology, Prince of Wales Hospital, Shatin, Hong Kong
66473926
queenapoon@cuhk.edu.hk
Department of Orthopaedics and Traumatology, The Chinese University of Hong Kong
Hong Kong
Prof. Kevin HO Ki Wai
Department of Orthopaedics and Traumatology, The Chinese University of Hong Kong
26322715
kevinho@cuhk.edu.hk
Department of Orthopaedics and Traumatology, The Chinese University of Hong Kong
Hong Kong
A Randomized Control Clinical Trial to Evaluate the Efficacy of Intra-articular Injections of Mesenchymal Stem Cells versus Hyaluronic Acid in Patients Affected by Osteoarthritis of the Knee
RCT mesenchymal stem cells versus hyaluronic acid in OA knee
比較膝關節内注射間充質幹細胞及透明質酸用於治療膝關節炎的效用
RCT mesenchymal stem cells versus hyaluronic acid in OA knee
HKSAR
Yes
2015-06-17
Joint CUHK-NTEC Clinical Research Ethics Committee
2014.279-T
Degenerative osteoarthritis of the knee
Drug
autologous bone marrow derived mesenchymal stem cells and hyaluronic acid
Injection
6 ml in single-dosage
Single-dosage injection in time
Single dosage
To compare the effect of mesenchymal stem cells and hyaluronic acid on treating osteoarthritis of the knee, after intra-articular injection of both
Injection
6 ml in single-dosage
Single-dosage injection in time
Single-dose treatment
Patients must comply with all the following criteria in order to be included in the study
1.Male and female subjects aged between 18 and < 65;
2.All patients must provide their written consent;
3.All patients must be affected by primary osteoarthritis of the knee (according to ACR – American College of Rheumatology – classification); In case a patient shows a bilateral OA, it will be included and treated for both knees;
4.All patients must have pain symptoms since at least 2 months;
5. All patients must experience, during the inclusion visit (T0), a pain level higher than or equal to 5.0 cm on a VAS scale of 10 cm;
6.All patients should have at least 8 years of school education;
7.Radiological evidence of osteoarthritis with Kellgren and Lawrence grade 2 and 3
The presence of one or more of the following criteria will exclude the patient from the study:
1.Patients with previous cases of alcoholism or drug abuse;
2.Pregnancy and breast-feeding;
3.Presence of serious pathologies;
4.Hypersensitivity towards hyaluronic acid;
5.Intra-articular infiltrations of hyaluronic acid or steroids that are in the process of being administered or that have been interrupted since less than 3 months;
6.Steroid-based systemic therapy in progress or interrupted since less than 1 month and/or anti-clotting drugs;
7.History of fractures and/or severe traumas of the knee bone;
8.Significant hematologic diseases;
9.Non-consenting patients who have not provided the written Informed Consent;
10.Mechanical instability, ligamentous laxity/deficiency and gross deformity;
11.Isolated meniscal tear without evident of osteoarthritis.
18
65
Both Male and Female
Interventional
Randomized
Mesenchymal Stem Cells vs Hyaluronic Acid Injection for Osteoarthritis Knee
Active
Open label
Parallel
1
2015-12-01
20
Complete
Functional osteoarthritis scores including WOMAC,KSS and KSFS, SF-36 and VAS pain scores will be assessed at 2 weeks, 3 months, 6 months, 9 months and 12 months post-operation;
Radiologic knee osteoarthritis will be assessed by MRI-and X-ray before operation, 3 months and 12 months post-operation;
Adverse event will be monitored during the study.
Analgesic/NSAIDs consumption;
Crackling sounds with movement (subjective evaluation);
Per-articular swelling (thigh and knee circumference evaluation).
2020-05-14
ChiCTR-IOR-15006942
2015-08-20
|
|
|
|
---|---|---|---|
No documents yet. |