Traditional Chinese and Western Medicine for Knee Osteoarthritis

Knee Osteoarthritis Clinical Trial

— TCMWMKOA  

Official title:

Investigation of Traditional Chinese and Western Medicine in the Real World of Knee Osteoarthritis: A Multicenter Cohort Study

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05133934
• Other study ID #: TCMWM-KOA
• Status: Recruiting
• Start date: October 1, 2021
• Est. completion date: December 2024

Study information

• Verified date: November 2021
• Source: Hong Kong Baptist University
• Contact: Linda Zhong, MD, PhD
• Phone: 34116523
• Email: ldzhong0305[@]gmail.com
• Is FDA regulated: No
• Study type: Observational [Patient Registry]

Clinical Trial Summary

A cohort study will be used to collect patient data, analyze the clinical characteristics, traditional Chinese medicine (TCM) syndromes, and treatment of knee osteoarthritis (KOA) in China to accumulate clinical data and clarify the status of KOA in the real world background. It will lay a clinical foundation for further study of KOA in the future, and bring certain clinical value for Chinese patients with KOA.

Description:

This is a multicenter cohort study. It is planned to carry out multicenter investigation and research on the current situation of knee osteoarthritis in the real world, conduct large-scale investigation on the clinical population of patients with knee osteoarthritis, and establish a research, quality control, data management and statistical analysis platform for the clinical practical application of knee osteoarthritis and hospital registration. This study aims to discover the current clinical characteristics, TCM syndromes, and treatment status of patients with knee osteoarthritis in China, and provide reliable data support for the clinical treatment of KOA. It is estimated that 5000 patients from 23 centers across China will be recruited. Various demographic and disease-related information will be documented, including name, gender, age, job category, disease course, medical consultation experience, treatment satisfaction and so on. Patients will also complete a series of scales, containing Visual Analog Scale (VAS) Score, Knee Injury and Osteoarthritis Outcome Score (KOOS), Western Ontario and McMaster Universities (WOMAC) Osteoarthritis Index, 9-item patient health questionnaire (PHQ-9), SF-12 quality of life, TCM syndrome score sheet, etc. The primary outcome will be the pain (rest pain) VAS, KOOS, WOMAC knee osteoarthritis index score and TCM syndrome score. Secondary outcomes include patient's knee joint function examination, X-ray examination results, blood routine, biochemical indicators and pharmacoeconomic data.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 5000
• Est. completion date: December 2024
• Est. primary completion date: October 2024
• Accepts healthy volunteers: No
• Gender: All
• Age group: 50 Years to 80 Years

Eligibility

Inclusion Criteria:

1. The patient has repeated knee joint pain in the past month;

2. X-ray film (standing position or weight-bearing position) shows narrowing of the joint space, subchondral bone sclerosis and/or cystic degeneration, and osteophyte formation on the joint edges;

3. Age =50 years old;

4. Morning stiffness time =30min;

5. There is bone friction sound (sensation) during activity. Patients who meet the diagnostic criteria 1 + (any 2 of 2, 3, 4, 5) can be diagnosed as KOA. Exclusion Criteria: Patients who do not meet the diagnostic criteria for knee osteoarthritis

Related Conditions & MeSH terms

• Knee Osteoarthritis
• Osteoarthritis
• Osteoarthritis, Knee

Intervention

Other:
• Observational
A cohort study will be used to collect patient data, analyze the clinical characteristics, TCM syndromes, and treatment of knee osteoarthritis in China

Locations

Country	Name	City	State
Hong Kong	Hong Kong	Kowloon Tong	Kowloon

Sponsors (24)

Lead Sponsor

Collaborator

Hong Kong Baptist University

Affiliated Hospital of Shandong University of Traditional Chinese Medicine Hospital, China-Japan Friendship Hospital, Dongzhimen Hospital, Beijing University of Chinese Medicine, First Affiliated Hospital of Harbin Medical University, First Affiliated Hospital, Helongjiang University of Chinese Medicine, Guanghua Hospital Affiliated to Shanghai University of Traditional Chinese Medicine, Henan Province Hospital of TCM, Integrated Hospital of Traditional Chinese Medicine, Southern Medical University, Jiangsu Province Hospital of Chinese Medicine, Nanfang Hospital of Southern Medical University, Ruijin Hospital, Shanghai Municipal Hospital of Traditional Chinese Medicine Affiliated to Shanghai University of TCM, Shanghai University of Traditional Chinese Medicine, Shenzhen Traditional Chinese Medicine Hospital, ShuGuang Hospital, The First Affiliated Hospital of Nanchang University, The First Affiliated Hospital with Nanjing Medical University, The First Affiliated Hospital, Guangzhou University of Traditional Chinese Medicine, The Second Clinical Medical College of Zhejiang University of Traditional Chinese Medicine, The Second People's Hospital Affiliated to Fujian University of Traditional Chinese Medicine, The Southwest Hospital of AMU, Traditional Chinese Medicine Hospital of Xinjiang Uygur Autonomous Region, Yueyang Hospital of Integrated Traditional Chinese and Western Medicine, Shanghai University of TCM

Country where clinical trial is conducted

Hong Kong, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Patient-assessed Pain (rest pain) Visual Analog Scale (VAS) score	The pain VAS is a continuous scale comprised of a horizontal (HVAS) or vertical (VVAS) line, 10 centimeters (100 mm) in length, each end of this scale is an extreme label of the symptom, "no pain" (corresponding to the scale of 0) and "pain too intense to be tolerated" (corresponding to the scale of 100). Respondents indicate their degree of acceptance to a statement by specifying a point on the continuous scale in between two endpoints.; Using a ruler, the score is determined by measuring the distance (mm) on the 10-cm line between the "no pain" anchor and the patient's mark, providing a range of scores from 0-100.; A higher score indicates greater pain intensity.	1 month
Primary	The Knee Injury and Osteoarthritis Outcome Score (KOOS)	KOOS is a self-administered, knee-specific instrument to assess the patients' opinion about their knee and associated problems.; The KOOS evaluates both short-term and long-term consequences of knee injury. It holds 42 items in 5 separately scored subscales: Symptoms & Stiffness (7 items); Pain (9 items); Function in daily living (ADL Function) (17 items); Sport and Recreation Function (5 items); Quality of Life (4 items); A Likert scale is used and all items have 5 possible answer options scored from 0 (No Problems) to 4 (Extreme Problems) and each of the 5 scores is calculated as the sum of the items included. Scores are transformed to a 0-100 scale, with zero representing extreme knee problems and 100 representing no knee problems as common in orthopedic assessment scales and generic measures. Scores between 0 and 100 represent the percentage of total possible score achieved.	1 month
Primary	WOMAC Knee Osteoarthritis Index Score	WOMAC knee osteoarthritis index is a self-administered questionnaire consisting of 24 items divided into 3 subscales: Pain (5 items): Stiffness (2 items): Physical Function (17 items); A Likert scale is used and all items have 5 possible answer options: none (0), mild (1), moderate (2), severe (3), and extreme (4).; A total WOMAC score is created by summing the items for all three subscales (0-96), and higher scores indicate worse pain, stiffness, and functional limitations.	1 month
Primary	TCM Syndrome Differentiation and Symptom Score	Patients' health as characterized by CM diagnostic pattern & clinical characteristics is recorded using the standard of TCM syndrome differentiation that adopts the 2019 Chinese Society of Chinese Medicine Clinical Diagnosis and Treatment Guidelines for TCM Orthopedics and Traumatology - Knee Arthritis (Knee Osteoarthritis) Syndrome Differentiation Standard (cold-damp arthralgia syndrome, damp-heat arthralgia syndrome, stagnation of Qi and blood stasis syndrome, liver and kidney deficiency syndrome, and qi and blood weakness syndrome)	1 month
Secondary	Knee Joint Function	knee joint's function Questionnaire	1 month
Secondary	Morning Stiffness Time (in minutes)	Morning stiffness time (in minutes) is self recorded by patients daily when they wake up in the morning, to assess the severity of the stiffness.; Prolonged morning stiffness that lasts more than an hour and up to several hours suggest worsened osteoarthritis or other inflammatory types of arthritis.	1 month
Secondary	9-Item Patient Health Questionnaire (PHQ-9),	PHQ-9 is a multipurpose instrument for screening, diagnosing, monitoring and measuring the severity of depression.; The severity of depression is categorized into mild, moderate, moderately severe and severe depression. The final question on the PHQ-9 screens for the presence and duration of suicide ideation.	1 month
Secondary	12-Item Short Form Survey (SF-12) for Quality of Life of Patients	The SF-12 is a self-reported quality of life measure to be scored by a researcher, to assess the impact of health on patients' everyday life, and keeps track of how patients feel and how well they are able to do their usual activities.; It consists of 12 questions measuring eight domains of health, including physical functioning, role physical, bodily pain, general health, vitality, social functioning, role emotional and mental health. These health domain scores are aggregated into the physical component summary (PCS) score and the mental component summary (MCS) score.; Higher component summary scores indicate better health and better health-related quality of life (HRQoL).	1 month
Secondary	Complete blood count (CBC)	CBC is done to help evaluate red and white blood cells and hemoglobin, and to monitor the side effects of some OA treatments	1 month
Secondary	C-reactive Protein (CRP)	CRP is done to detect inflammation and test for the activity of the disease; an increased level of CRP suggests other forms of inflammatory arthritis, such as rheumatoid arthritis (RA) instead of osteoarthritis.	1 month
Secondary	Erythrocyte Sedimentation Rate (ESR)	The ESR rate increases as a result of any cause or focus of inflammation. ESR is done to detect inflammation in the body; ESR will be increased in other forms of inflammatory arthritis, such as RA but not in osteoarthritis.	1 month
Secondary	Liver Function	Liver function test is done to assess patients' liver function, as abnormal liver function tests are often seen in patients with inflammatory arthritis.	1 month
Secondary	Kidney Function	Kidney function test is done to assess patients' kidney function, as kidney toxicity is a potential side effect of some arthritis medications.	1 month
Secondary	Urine Routine	Urine test is done to assess patients' kidney function, as kidney toxicity is a potential side effect of some arthritis medications.	1 month
Secondary	Examination of X-Ray	X-rays of the affected knee joints to assess the loss of cartilage, bone damage, bone spurs, and narrowing of the joint space using following grading scale: Grade 0 (normal); Grade I (suspicious narrowing of joint space, possibly osteophytes); Grade II (obvious osteophytes, slightly narrowed joint space); Grade III (moderate osteophytes, more obviously narrowed joint space, slightly sclerotic subchondral bone); Grade IV (large number of osteophytes, significantly narrowed joint space, extremely obvious sclerosis changes, joints hypertrophy and obvious deformities)	1 month