To Assess the Efficacy of Collagen Supplement in Osteoarthritis
Primary Purpose
Knee Osteoarthritis
Status
Completed
Phase
Not Applicable
Locations
India
Study Type
Interventional
Intervention
Collagen Supplement
Glucosamine chondroitin
Placebo
Sponsored by

About this trial
This is an interventional other trial for Knee Osteoarthritis
Eligibility Criteria
Inclusion Criteria:
- Male & female aged ≥ 40 to ≤ 65 years suffering from knee joint pain for at least 3 months prior to screening.
- BMI ≥ 18.5 and ≤ 29.9 kg/m2.
- Non-vegetarians (Regardless of whether they eat chicken, fish, goat mutton, pork, beef or eggs).
- Screening Visual Analogue (VAS) scores for knee joint pain ≥ 60 on a 100-point scale.
- Radiographic evidence of grade II/III knee OA based on one of following criteria.
- Participants willing to stop the restricted supplements and medications prior to inclusion and throughout the study period.
- Participants willing to stop any home-based remedies or any other form of topical products intended for knee joint pain relief or any other reason for the entire study duration.
- Willing to stop the use of study designated rescue medication 48 hours prior to all assessment visits.
- Willing to abstain from food containing type II collagen only from cartilage, e.g. chicken, fish, beef, pork, etc. 48 hours prior to all assessment visits.
Exclusion Criteria:
- Prior or ongoing medical conditions (e.g. concomitant illness, psychiatric disorders, etc.), abnormal medical history or physical findings.
- Participants with history of type II diabetes and uncontrolled hypertension.
- Fasting Blood glucose > 125 mg/dl
- Systolic blood pressure ≥ 140 mmHg and/or diastolic blood pressure ≥ 90 mmHg.
- Radiographic evidence of Grade I or Grade IV OA based on the KL radiographic criteria for osteoarthritis.
- Any history of trauma, fractures or surgery to the index joint.
- Any planned surgery (diagnostic or therapeutic intervention) to the index joint during the participation in the study.
- Participants with deformity of the knee joint.
- Participants with a diagnosed condition which may involve or involves the index joint that includes but is not limited to known rheumatic or inflammatory conditions such as rheumatoid arthritis, osteomyelitis, osteoporosis, gout, and bone metastasis.
- Other pathologic lesions on X-rays of the knee.
- Current smokers or chronic alcoholics
Sites / Locations
- Dr. Randive's knee and spine clinic
- PKC Hospital
- Dr Sonawane orthopedic clinic
- Rainbow Multispeciality hospital and trauma center
- Shubham Sudbhawana Super Specialty Hospital
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Active Comparator
Other
Placebo Comparator
Arm Label
Collagen Supplement
Glucosamine chondroitin
Placebo
Arm Description
Three capsules post-breakfast Three capsules post-dinner
Three capsules post-breakfast Three capsules post-dinner
Three capsules post-breakfast Three capsules post-dinner
Outcomes
Primary Outcome Measures
modified Western Ontario and McMaster Score
Effect of consumption of IP on Joint health as assessed by the change in the (mWOMAC) total score from baseline and when compared with the placebo. [From baseline to 84 days] High score defines worst outcome and low score defines better oucome.
Secondary Outcome Measures
EQ-5D-5L
Effect of consumption of IP on Joint health as assessed by the change in the EQ-5D-5L from baseline and when compared with the placebo. [From baseline to 84 days]
interleukin-6 (IL - 6)
Effect of consumption of IP on Joint inflammation as assessed by the change in the inflammatory biomarker interleukin-6 (IL-6) concentration from baseline and when compared with the placebo. [From baseline to 84 days]
Full Information
NCT ID
NCT04470336
First Posted
July 8, 2020
Last Updated
April 29, 2021
Sponsor
Vedic Lifesciences Pvt. Ltd.
1. Study Identification
Unique Protocol Identification Number
NCT04470336
Brief Title
To Assess the Efficacy of Collagen Supplement in Osteoarthritis
Official Title
A Double-blind, Placebo-controlled, Randomized, Parallel Study to Assess the Efficacy of Collagen Supplement in Osteoarthritis
Study Type
Interventional
2. Study Status
Record Verification Date
March 2021
Overall Recruitment Status
Completed
Study Start Date
July 9, 2020 (Actual)
Primary Completion Date
February 24, 2021 (Actual)
Study Completion Date
April 12, 2021 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Vedic Lifesciences Pvt. Ltd.
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
Collagen Supplement is a natural ingredient that contains undenatured collagen derived from chicken sternum. Collagen Supplement is efficacious and safe as compared to placebo and efficacy is also comparable to glucosamine plus chondroitin for treatment of of knee Osteoarthritis
Detailed Description
Osteoarthritis (OA) is a chronic progressive degenerative disease involving thinning of cartilage in movable joints that leads to friction between bones creating pain, stiffness, and abnormal movement. It is estimated to affect more than 20% of the population over the age of 60 years and is considered to be a major cause of morbidity, disability, and limitations on the quality of life. In India, studies have reported the prevalence of 22% to 39%, with OA being 2nd most common rheumatological disorder. , As global life expectancy increases, the prevalence of OA is expected to rise further ultimately resulting in a greater burden for healthcare. Currently, the management has largely been palliative, focusing on the alleviation of symptoms.
The principles of OA treatments primarily are to alleviate pain and stiffness and maintain function. The current treatment guidelines recommend a combination of physical therapy, use of analgesia with Acetaminophen or NSAIDs, and surgical intervention when deemed necessary. While medications slow the progression of OA and other inflammatory conditions, no proven disease-modifying agents for the treatment of knee OA currently exists. The majority of individuals are successfully managed with a combination of the aforementioned treatments, but there is still a significant group of patients in whom these treatments do not provide adequate relief. Furthermore, there remains a lack of treatments that have demonstrated effectiveness in stopping or reversing the degenerative process. , Besides, there are considerable side effects associated with the use of these drugs. As a result, OA sufferers have turned to natural nutraceuticals to ease their pain and discomfort.
In recent years, several novel agents have emerged as potential treatment alternatives to improve pain, stiffness, and function with the possibility of altering disease progression. These products are commonly used because they are well tolerated and considered safe. Among the OA patients, glucosamine and chondroitin are most commonly used and have shown to considerably reduce the pain associated with arthritis. From the nutraceutical point of view, there is a growing interest in Collagen Supplement as a solution for the treatment of OA. The Collagen Supplement has been studied extensively in both animals as well as human clinical studies. , Among animal studies, a study in the rat model of OA reported several benefits after treatment, suggesting its potential for the prevention of worsening of articular cartilage damage. In another study, porcine Collagen Supplement administration demonstrated a significant reduction of pain intensity. Also, a lower dose regimen showed meaningful pain reduction indicating its protective effect on the cartilage. Furthermore, several studies have evaluated the efficacy and safety of Collagen Supplement in individuals suffering from chronic OA. Crowley and colleagues showed that supplementation of Collagen Supplement for three months is more efficacious as compared to the combination of glucosamine plus chondroitin. In another study, 6-month administration of the Collagen Supplement significantly reduced pain, stiffness, and physical functioning as compared to glucosamine hydrochloride plus chondroitin sulfate group of participants with knee OA.
Based on the available evidence it is clear that Collagen Supplement is effective in improving joint discomfort associated with OA. Moreover, collagen products are also recognized as safe components of pharmaceutical and foods by the US Food and Drugs Administration Center for Food Safety and Nutrition. Hence, considering its symptomatic benefits, the structural effect on the cartilage and its important role in bone structure, Collagen Supplement is thought to be a viable alternative for OA patients. , Therefore, the present study aimed to evaluate the safety and efficacy of an collagen supplementation in participants suffering from knee OA. Study volunteers will be supplemented with Collagen Supplement, an collagen product for 12 weeks and assessed as per study designated efficacy and safety variables. Also, the efficacy and efficacy of Collagen Supplement will be compared with Glucosamine HCL plus chondroitin sulfate and placebo as per the set study intervals.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Knee Osteoarthritis
7. Study Design
Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
102 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Collagen Supplement
Arm Type
Active Comparator
Arm Description
Three capsules post-breakfast Three capsules post-dinner
Arm Title
Glucosamine chondroitin
Arm Type
Other
Arm Description
Three capsules post-breakfast Three capsules post-dinner
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Three capsules post-breakfast Three capsules post-dinner
Intervention Type
Other
Intervention Name(s)
Collagen Supplement
Intervention Description
Three capsules post-breakfast Three capsules post-dinner
Intervention Type
Other
Intervention Name(s)
Glucosamine chondroitin
Intervention Description
Three capsules post-breakfast Three capsules post-dinner
Intervention Type
Other
Intervention Name(s)
Placebo
Intervention Description
Three capsules post-breakfast Three capsules post-dinner
Primary Outcome Measure Information:
Title
modified Western Ontario and McMaster Score
Description
Effect of consumption of IP on Joint health as assessed by the change in the (mWOMAC) total score from baseline and when compared with the placebo. [From baseline to 84 days] High score defines worst outcome and low score defines better oucome.
Time Frame
Day0 Day 28 Day 56 Day 84
Secondary Outcome Measure Information:
Title
EQ-5D-5L
Description
Effect of consumption of IP on Joint health as assessed by the change in the EQ-5D-5L from baseline and when compared with the placebo. [From baseline to 84 days]
Time Frame
Day 0 and Day 84
Title
interleukin-6 (IL - 6)
Description
Effect of consumption of IP on Joint inflammation as assessed by the change in the inflammatory biomarker interleukin-6 (IL-6) concentration from baseline and when compared with the placebo. [From baseline to 84 days]
Time Frame
Day 0 Day 84
10. Eligibility
Sex
All
Minimum Age & Unit of Time
40 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Male & female aged ≥ 40 to ≤ 65 years suffering from knee joint pain for at least 3 months prior to screening.
BMI ≥ 18.5 and ≤ 29.9 kg/m2.
Non-vegetarians (Regardless of whether they eat chicken, fish, goat mutton, pork, beef or eggs).
Screening Visual Analogue (VAS) scores for knee joint pain ≥ 60 on a 100-point scale.
Radiographic evidence of grade II/III knee OA based on one of following criteria.
Participants willing to stop the restricted supplements and medications prior to inclusion and throughout the study period.
Participants willing to stop any home-based remedies or any other form of topical products intended for knee joint pain relief or any other reason for the entire study duration.
Willing to stop the use of study designated rescue medication 48 hours prior to all assessment visits.
Willing to abstain from food containing type II collagen only from cartilage, e.g. chicken, fish, beef, pork, etc. 48 hours prior to all assessment visits.
Exclusion Criteria:
Prior or ongoing medical conditions (e.g. concomitant illness, psychiatric disorders, etc.), abnormal medical history or physical findings.
Participants with history of type II diabetes and uncontrolled hypertension.
Fasting Blood glucose > 125 mg/dl
Systolic blood pressure ≥ 140 mmHg and/or diastolic blood pressure ≥ 90 mmHg.
Radiographic evidence of Grade I or Grade IV OA based on the KL radiographic criteria for osteoarthritis.
Any history of trauma, fractures or surgery to the index joint.
Any planned surgery (diagnostic or therapeutic intervention) to the index joint during the participation in the study.
Participants with deformity of the knee joint.
Participants with a diagnosed condition which may involve or involves the index joint that includes but is not limited to known rheumatic or inflammatory conditions such as rheumatoid arthritis, osteomyelitis, osteoporosis, gout, and bone metastasis.
Other pathologic lesions on X-rays of the knee.
Current smokers or chronic alcoholics
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Dr. Shalini Srivastava, MD - Med.
Organizational Affiliation
Vedic Life Sciences Pvt. Ltd.
Official's Role
Study Director
Facility Information:
Facility Name
Dr. Randive's knee and spine clinic
City
Mumbai
State/Province
Maharashtra
ZIP/Postal Code
400093
Country
India
Facility Name
PKC Hospital
City
Mumbai
State/Province
Maharashtra
ZIP/Postal Code
400705
Country
India
Facility Name
Dr Sonawane orthopedic clinic
City
Mumbai
State/Province
Maharashtra
ZIP/Postal Code
400709
Country
India
Facility Name
Rainbow Multispeciality hospital and trauma center
City
Navi Mumbai
State/Province
Maharashtra
ZIP/Postal Code
400708
Country
India
Facility Name
Shubham Sudbhawana Super Specialty Hospital
City
Varanasi
State/Province
Uttar Pradesh
ZIP/Postal Code
221005
Country
India
12. IPD Sharing Statement
Learn more about this trial
To Assess the Efficacy of Collagen Supplement in Osteoarthritis
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