Osteoarthritis, Knee Clinical Trial
Official title:
The Efficacy of TGF for Treating Osteoarthritis of the Knee: A Randomized Double-blind Controlled Trial
This study is to evaluate the efficacy of herbal formula TGF treating knee joint
osteoarthritis(KOA) and its biochemical mechanism. The study design is a parallel randomized,
placebo-controlled, double-blind clinical trial includes 180 patients with KOA. The patients
are random allocated into study group(taking TGF) and control group(taking 1/20 TGF). After
the 12 weeks treatment course, another 4 weeks is to follow-up the condition without
medication. Assessments will be performed before and after treatment and the end of follow-up
period.
The inclusion criteria are (1) age between 50~75 years old, (2) diagnosis of osteoarthritis:
The Clinical/Radiographic classification criteria of American College of Rheumatology,
American College of Rheumatology, (3) chronic knee pain over 3 months. The exclusion criteria
are (1) the past history with systemic joint disease, such as autoimmune disease, (2) the
patient with history of knee surgery or waiting for the total knee replacement, (3) any
disease that affect the function of lower extremities, such as trauma, tumor or compensation
of abnormal posture, (4) the condition that cannot participate this study, (5) the subjects
non-compliance with the protocol.
The Assessments including primarily the WOMAC (VAS version, 3.1), VAS and the used dosage of
Celebrex before and after treatment. The secondary assessments are (1) X ray, (2)
Constitution in Chinese Medicine Questionnaire, (3) Short From-36, (4) erythrocyte
sedimentation rate and C reactive protein, (5) Biomarkers: C-telopeptide of type II collagen,
cartilage oligomeric matrix protein, Osteocalcin, Leptin, Interleukin-1, Interleukin-6,
matrix metalloproteinase-3, matrix metalloproteinase-13, ADAMTS-4, transglutaminase-2, and
(6) metabolomics.
Status | Not yet recruiting |
Enrollment | 180 |
Est. completion date | December 31, 2021 |
Est. primary completion date | December 31, 2021 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 50 Years to 75 Years |
Eligibility |
Inclusion Criteria: 1. age between 50~75 years old 2. diagnosis of osteoarthritis: The Clinical/Radiographic classification criteria of American College of Rheumatology, ACR 3. chronic knee pain over 3 months. Exclusion Criteria: 1. the past history with systemic joint disease, such as autoimmune disease 2. the patient with history of knee surgery or waiting for the total knee replacement 3. any disease that affect the function of lower extremities, such as trauma, tumor or compensation of abnormal posture 4. the condition that cannot participate this study 5. the subjects non-compliance with the protocol |
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
China Medical University Hospital |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Western Ontario & McMaster Universities Osteoarthritis Index | This scale is the VAS version, 3.1 and divided into three sub-scales -- pain, stiffness and function. Pain (5 items): during walking, using stairs, in bed, sitting or lying, and standing. Stiffness (2 items): after first waking and later in the day. Physical Function (17 items): stair use, rising from sitting, standing, bending, walking, getting in / out of a car, shopping, putting on / taking off socks, rising from bed, lying in bed, getting in / out of bath, sitting, getting on / off toilet, heavy household duties, light household duties. Each item has 0-100 mm to evaluate the status and the higher values represent a worse outcome. These three sub-scales were summed to a total score (0-2400 mm). | Change from Baseline WOMAC VAS version 3.1 at 3 months | |
Primary | Visual Analogue Scale for pain | To evaluate the status of knee pain when check point. Using 0-100 mm scale is to evaluate knee pain by visual analogue scale. "0" is no pain and "100" is the worst pain that subjects had experienced before. The subject gives the value under the moment of check point. | Change from Baseline Visual Analogue Scale for pain at 3 months | |
Primary | the used dosage of Celebrex | To evaluate the dosage of Celebrex when check point | Change from Baseline the used dosage of Celebrex at 3 months | |
Primary | Western Ontario & McMaster Universities Osteoarthritis Index | This scale is the VAS version, 3.1 and divided into three sub-scales -- pain, stiffness and function. Pain (5 items): during walking, using stairs, in bed, sitting or lying, and standing. Stiffness (2 items): after first waking and later in the day. Physical Function (17 items): stair use, rising from sitting, standing, bending, walking, getting in / out of a car, shopping, putting on / taking off socks, rising from bed, lying in bed, getting in / out of bath, sitting, getting on / off toilet, heavy household duties, light household duties. Each item has 0-100 mm to evaluate the status and the higher values represent a worse outcome. These three sub-scales were summed to a total score (0-2400 mm). | Change from Baseline WOMAC VAS version 3.1 at 4 months | |
Primary | Visual Analogue Scale for pain | To evaluate the status of knee pain when check point. Using 0-100 mm scale is to evaluate knee pain by visual analogue scale. "0" is no pain and "100" is the worst pain that subjects had experienced before. The subject gives the value under the moment of check point. | Change from Baseline Visual Analogue Scale for pain at 4 months | |
Primary | the used dosage of Celebrex | To evaluate the dosage of Celebrex when check point | Change from Baseline the used dosage of Celebrex at 4 months | |
Secondary | X ray | knee joint that associated with this study | Change from Baseline X ray at 3 months | |
Secondary | X ray | knee joint that associated with this study | Change from Baseline X ray at 4 months | |
Secondary | Constitution in Chinese Medicine Questionnaire, CCMQ | For evaluating the constitution. This scale (Constitution in Chinese Medicine Questionnaire) includes nine constitutions and each constitution has 6-8 items that used 1-5 points to evaluate the degree. "1" means "better" and "5" means "worse". The transformed points is equal to [(original points - the number of items)/(the number of itmes*4) ]*100. | Change from Baseline CCMQ at 3 months | |
Secondary | Constitution in Chinese Medicine Questionnaire, CCMQ | For evaluating the constitution. This scale (Constitution in Chinese Medicine Questionnaire) includes nine constitutions and each constitution has 6-8 items that used 1-5 points to evaluate the degree. "1" means "better" and "5" means "worse". The transformed points is equal to [(original points - the number of items)/(the number of itmes*4) ]*100. | Change from Baseline CCMQ at 4 months | |
Secondary | WHOQOL-BREF | For evaluating the quality of life. This scale is "World Health Organization Quality of Life - BREF". It contains 4 domains (Physical health, Psychological, Social relationships and Environment) and 26 items ("1" means "worse" and "5" means "better"). This scale used the following steps to calculate the transformed points: 1.Check all 26 items from assessment have a range of 1-5, 2.Reverse 3 negatively phrased items, 3.Compute domain scores, 4. Delete cases with >20% missing data, 5.Check domain scores. | Change from Baseline WHOQOL at 3 months | |
Secondary | WHOQOL | For evaluating the quality of life. This scale is "World Health Organization Quality of Life - BREF". It contains 4 domains (Physical health, Psychological, Social relationships and Environment) and 26 items ("1" means "worse" and "5" means "better"). This scale used the following steps to calculate the transformed points: 1.Check all 26 items from assessment have a range of 1-5, 2.Reverse 3 negatively phrased items, 3.Compute domain scores, 4. Delete cases with >20% missing data, 5.Check domain scores. | Change from Baseline WHOQOL at 4 months | |
Secondary | ESR | For evaluating the status of inflammation. Erythrocyte Sedimentation Rate (ESR) actually measures the rate of fall (sedimentation) of erythrocytes (red blood cells) in a sample of blood that has been placed into a tube. Results are reported as the millimeters of clear fluid (plasma) that are present at the top portion of the tube after one hour. The higher value means more inflammation. | Change from Baseline ESR at 3 months | |
Secondary | ESR | For evaluating the status of inflammation. Erythrocyte Sedimentation Rate (ESR) actually measures the rate of fall (sedimentation) of erythrocytes (red blood cells) in a sample of blood that has been placed into a tube. Results are reported as the millimeters of clear fluid (plasma) that are present at the top portion of the tube after one hour. The higher value means more inflammation. | Change from Baseline ESR at 4 months | |
Secondary | CTX-II | This study uses ELISA kit to measure the concentraion (pg/ml) of C-Telopeptide of Type II Collagen (CTX-II) . | Change from Baseline CTX-II at 3 months | |
Secondary | CTX-II | This study uses ELISA kit to measure the concentraion (pg/ml) of C-Telopeptide of Type II Collagen (CTX-II) . | Change from Baseline biomarkers at 4 months | |
Secondary | COMP | This study uses ELISA kit to measure the concentraion (ng/ml) of Cartilage Oligomeric Matrix Protein (COMP) . | Change from Baseline biomarkers at 3 months | |
Secondary | COMP | This study uses ELISA kit to measure the concentraion (ng/ml) of Cartilage Oligomeric Matrix Protein (COMP) . | Change from Baseline biomarkers at 4 months | |
Secondary | Osteocalcin | This study uses ELISA kit to measure the concentraion (ng/ml) of Osteocalcin . | Change from Baseline biomarkers at 3 months | |
Secondary | Osteocalcin | This study uses ELISA kit to measure the concentraion (ng/ml) of Osteocalcin . | Change from Baseline biomarkers at 4 months | |
Secondary | Leptin | This study uses ELISA kit to measure the concentraion (pg/ml) of Leptin. | Change from Baseline biomarkers at 3 months | |
Secondary | Leptin | This study uses ELISA kit to measure the concentraion (pg/ml) of Leptin. | Change from Baseline biomarkers at 4 months | |
Secondary | IL-1 | This study uses ELISA kit to measure the concentraion (ng/ml) of interleukin-1 (IL-1). | Change from Baseline biomarkers at 3 months | |
Secondary | IL-1 | This study uses ELISA kit to measure the concentraion (ng/ml) of interleukin-1 (IL-1). | Change from Baseline biomarkers at 4 months | |
Secondary | IL-6 | This study uses ELISA kit to measure the concentraion (ng/ml) of interleukin-6 (IL-6). | Change from Baseline biomarkers at 3 months | |
Secondary | IL-6 | This study uses ELISA kit to measure the concentraion (ng/ml) of interleukin-6 (IL-6). | Change from Baseline biomarkers at 4 months | |
Secondary | MMP-3 | This study uses ELISA kit to measure the concentraion (ng/ml) of matrix metalloproteinase-3 (MMP-3). | Change from Baseline biomarkers at 3 months | |
Secondary | MMP-3 | This study uses ELISA kit to measure the concentraion (ng/ml) of matrix metalloproteinase-3 (MMP-3). | Change from Baseline biomarkers at 4 months | |
Secondary | MMP-13 | This study uses ELISA kit to measure the concentraion (pg/ml) of matrix metalloproteinase-13 (MMP-13). | Change from Baseline biomarkers at 3 months | |
Secondary | MMP-13 | This study uses ELISA kit to measure the concentraion (pg/ml) of matrix metalloproteinase-13 (MMP-13). | Change from Baseline biomarkers at 4 months | |
Secondary | ADAMTS-4 | This study uses ELISA kit to measure the concentraion (ng/ml) of a disintegrin and metalloproteinase with thrombospondin motifs-4 (ADAMTS-4). | Change from Baseline biomarkers at 3 months | |
Secondary | ADAMTS-4 | This study uses ELISA kit to measure the concentraion (ng/ml) of a disintegrin and metalloproteinase with thrombospondin motifs-4 (ADAMTS-4). | Change from Baseline biomarkers at 4 months | |
Secondary | TG-2 | This study uses ELISA kit to measure the concentraion (ng/ml) of Transglutaminase 2 (TG-2). | Change from Baseline biomarkers at 3 months | |
Secondary | TG-2 | This study uses ELISA kit to measure the concentraion (ng/ml) of Transglutaminase 2 (TG-2). | Change from Baseline biomarkers at 4 months | |
Secondary | Metabolomics | The metabolite of the drugs. This measurement used LC-MS to get the molecular weight of Chinese herbal metabolites form blood, urine and synovial fluid. This method can help to identify the active substance from the formula (TGF). Here, we cannot to know the exactly active substance that we will get. | Change from Baseline metabolomics at 3 months | |
Secondary | Metabolomics | The metabolite of the drugs. This measurement used LC-MS to get the molecular weight of Chinese herbal metabolites form blood, urine and synovial fluid. This method can help to identify the active substance from the formula (TGF). Here, we cannot to know the exactly active substance that we will get. | Change from Baseline metabolomics at 4 months | |
Secondary | Mitochondria research--mtDNA copy number | mtDNA copy number | Change from Baseline mtDNA copy number at 3 months | |
Secondary | Mitochondria research--mtDNA copy number | mtDNA copy number | Change from Baseline mtDNA copy number at 4 months | |
Secondary | Mitochondria research--the expression of messenger ribonucleic acid in Peroxisome proliferator-activated receptor-? coactivator-1a | the expression of mRNA in PGC-1a by quantitative polymerase chain reaction | Change from Baseline the expression of mRNA in PGC-1a at 3 months | |
Secondary | Mitochondria research--the expression of messenger ribonucleic acid in Peroxisome proliferator-activated receptor-? coactivator-1a | the expression of mRNA in PGC-1a by quantitative polymerase chain reaction | Change from Baseline the expression of mRNA in PGC-1a at 4 months | |
Secondary | Mitochondria research--the expression of messenger ribonucleic acid in Nuclear respiratory factor 1 | the expression of mRNA in NRF1 by quantitative polymerase chain reaction | Change from Baseline the expression of mRNA in NRF1 at 3 months | |
Secondary | Mitochondria research--the expression of messenger ribonucleic acid in Nuclear respiratory factor 1 | the expression of mRNA in NRF1 by quantitative polymerase chain reaction | Change from Baseline the expression of mRNA in NRF1 at 4 months | |
Secondary | Mitochondria research--the expression of messenger ribonucleic acid in mtTFA | the expression of mRNA in mtTFA by quantitative polymerase chain reaction | Change from Baseline the expression of mRNA in mtTFA at 3 months | |
Secondary | Mitochondria research--the expression of messenger ribonucleic acid in mtTFA | the expression of mRNA in mtTFA by quantitative polymerase chain reaction | Change from Baseline the expression of mRNA in mtTFA at 4 months | |
Secondary | Mitochondria research--the expression of protein in Peroxisome proliferator-activated receptor-? coactivator-1a | the expression of protein in PGC-1a by Western blotting | Change from Baseline the expression of protein in PGC-1a at 3 months | |
Secondary | Mitochondria research--the expression of protein in Peroxisome proliferator-activated receptor-? coactivator-1a | the expression of protein in PGC-1a by Western blotting | Change from Baseline the expression of protein in PGC-1a at 4 months | |
Secondary | Mitochondria research--the expression of protein in Nuclear respiratory factor 1 | the expression of protein in NRF1 by Western blotting | Change from Baseline the expression of protein in NRF1 at 3 months | |
Secondary | Mitochondria research--the expression of protein in Nuclear respiratory factor 1 | the expression of protein in NRF1 by Western blotting | Change from Baseline the expression of protein in NRF1 at 4 months | |
Secondary | Mitochondria research--the expression of protein in mtTFA | the expression of protein in mtTFA by Western blotting | Change from Baseline the expression of protein in mtTFA at 3 months | |
Secondary | Mitochondria research--the expression of protein in mtTFA | the expression of protein in mtTFA by Western blotting | Change from Baseline the expression of protein in mtTFA at 4 months | |
Secondary | Mitochondria research--anti-oxidant capacity | anti-oxidant capacity by OxiSelectTM Trolox Equivalent Antioxidant Capacity (TEAC) Assay Kit (ABTS) | Change from Baseline anti-oxidant capacity at 3 months | |
Secondary | Mitochondria research--anti-oxidant capacity | anti-oxidant capacity by OxiSelectTM Trolox Equivalent Antioxidant Capacity (TEAC) Assay Kit (ABTS) | Change from Baseline anti-oxidant capacity at 4 months | |
Secondary | hsCRP | For evaluating the status of inflammation. High-sensitivity C-reactive Protein is a protein that increases in the blood with inflammation and infection as well as following a heart attack, surgery, or trauma. Thus, it is one of several proteins that are often referred to as acute phase reactants. The high-sensitivity CRP test measures low levels of CRP in the blood to identify low levels of inflammation that are associated with risk of developing cardiovascular disease (CVD). | Change from Baseline CRP at 3 months | |
Secondary | hsCRP | For evaluating the status of inflammation. High-sensitivity C-reactive Protein is a protein that increases in the blood with inflammation and infection as well as following a heart attack, surgery, or trauma. Thus, it is one of several proteins that are often referred to as acute phase reactants. The high-sensitivity CRP test measures low levels of CRP in the blood to identify low levels of inflammation that are associated with risk of developing cardiovascular disease (CVD). | Change from Baseline CRP at 4 months |
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