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12week, randomized, double-blind, placebo-controlled clinical trial for the evaluation of the efficacy and safety of BST106 on Osteoarthritis

Not Applicable
Completed
Conditions
Diseases of the musculo-skeletal system and connective tissue
Registration Number
KCT0004238
Lead Sponsor
Inje University Seoul Paik Hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
All
Target Recruitment
80
Inclusion Criteria

Adult male and female between 40 years and 75 years
Patients diagnosed more than 30mm in VAS (Visual analogue scale)
Patients diagnosed grade I, II with kellgren & Lawrence grading scale in X-ray
Those who agree to the written consent of the applicant and who can cooperate with the necessary visits and related tests and surveys for the study process

Exclusion Criteria

(1) Subjects diagnosed with arthritis by specific factors othre than degenerative arthritis
(2) Joint spacing less than 2mm
(3) Subjects who are judged to have severe arthritis with bony spur, irregular articular surface and osteocystoma etc
(4) Subjects with clinically significant cardiovascilar, immune, infectious and neoplastic diseases
(5) Patients undergoing gastritis and gastric ulcers
(6) Subjects with resistant hypertension (Upper than 160/100mmHg, After 10 minutes rest)
(7) Subjects with resistant diabetes (Fasting glucose levels upper than 180mg/dl)
(8) TSH lower than 0.1µIU/ml or upper than 10 µIU/ml
(9) AST(GOT) and ALT(GPT) is at least 3 timesthe normal range
(10) Creatinine is at least twice the normal range
(11) Pregnant or nursing women
(12) Subjects who is on a diet Health Functional Foods and medicine to improve joint/cartilage health
(13) Subjects who are treated with mental disorders such as depression and schizophrenia.
(14) Oriental medicine treatment of acupuncture, moxibustion, cupping therapy, herbal medicine, etc. within 2 month prior to the study
(15) Participation in anothrt clinical trial within 2 month prior to the study
(16) Hypersensitivity or allergy to the test materials
(17) Participation who are judged to be unable to comply with the requirements of the test

Study & Design

Study Type
Interventional Study
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Total score of K-WOMAC (The western ontario and McMaster university osteoarthritis index)
Secondary Outcome Measures
NameTimeMethod
VAS (Visual analogue scale) and KSF-36 (Korean-short form health survey 36)
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