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Hyaluronic Acid Derivative
HYMOVIS for Osteoarthritis
N/A
Waitlist Available
Research Sponsored by Fidia Farmaceutici s.p.a.
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Symptomatic osteoarthritis of the knee.
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 26 weeks
Awards & highlights
Study Summary
The purpose of this study is to determine whether intra-articular hyaluronic acid provides symptomatic relief of osteoarthritis of the knee.
Eligible Conditions
- Osteoarthritis
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowTimeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 26 weeks
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~26 weeks
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Western Ontario and McMaster Universities Osteoarthritis (WOMAC) Pain Sub-score
Secondary outcome measures
Patient Global Assessment
Trial Design
2Treatment groups
Experimental Treatment
Placebo Group
Group I: HYMOVISExperimental Treatment1 Intervention
HYADD(TM) 4 Hydrogel Intra-Articular Injection
Group II: PlaceboPlacebo Group1 Intervention
Saline Intra-Articular Injection
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
HYMOVIS
2015
N/A
~50
Find a Location
Who is running the clinical trial?
Fidia Farmaceutici s.p.a.Lead Sponsor
32 Previous Clinical Trials
4,160 Total Patients Enrolled
5 Trials studying Osteoarthritis
1,184 Patients Enrolled for Osteoarthritis
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
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