Efficacy of Hydrolyzed Collagen and Undenatured Collagen Type II in Alleviating Pain in Patients With Knee Osteoarthritis
Collagen
+ Placebo
Arthritis+2
+ Joint Diseases
+ Musculoskeletal Diseases
Treatment Study
Summary
Study start date: November 1, 2023
Actual date on which the first participant was enrolled.This study is investigating the effectiveness of two types of collagen supplements, hydrolyzed collagen and undenatured type II collagen, in reducing knee pain for patients with osteoarthritis. Osteoarthritis is a common condition that causes joint pain and stiffness, often affecting the knees, which can significantly impact daily activities and quality of life. By exploring new treatment options like collagen supplements, the study aims to find alternative ways to manage pain and improve the lives of those suffering from this condition. Participants in this study are randomly assigned to one of two groups. One group receives a daily dose of 480 mg of hydrolyzed collagen and 20 mg of undenatured type II collagen, while the other group receives a placebo, which is a substance with no active ingredients. The main focus of the study is to measure changes in pain levels among the participants to evaluate the effectiveness of the collagen supplements. This controlled setup helps determine if these supplements can provide a real benefit in managing osteoarthritis pain.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.68 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Treatment Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.From 50 to 80 Years
Range of ages for which participants are eligible to join.Healthy volunteers not allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.2 intervention groups are designated in this study
50% chance of being blinded to the placebo group
Treatment Groups
Group I
ExperimentalGroup II
PlaceboStudy Objectives
Primary Objectives
Secondary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location