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Completed Not applicable Interventional Results available

A Study of the Safety and Effectiveness of Synvisc-One® (Hylan G-F 20) in Patients With Primary Osteoarthritis of the Hip

ClinicalTrials.gov ID: NCT01618708

Public ClinicalTrials.gov record NCT01618708. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 22, 2026, 9:22 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Pivotal, Multicenter, Double Blind Study of the Safety and Effectiveness of Synvisc-One® (Hylan G-F 20) in Patients With Mild to Moderate Primary Osteoarthritis of the Hip

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The primary objective of this study was to demonstrate any changes in assessments of pain for participants receiving Synvisc-One compared to control.

Study identification

NCT ID
NCT01618708
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Lead sponsor
Genzyme, a Sanofi Company
Industry
Enrollment
357 participants

Conditions and interventions

Interventions

Device

Eligibility (public fields only)

Age range
35 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Sep 2012 (Type not available)
Primary completion
Jun 2015 (Actual)
Completion
Jun 2015 (Actual)
Last update posted
Jul 11, 2016

2012 – 2015

United States locations

U.S. sites
45
U.S. states
24
U.S. cities
44
Facility City State ZIP Site status
Investigational Site Number 840025 Burmingham Alabama 35216 —
Investigational Site Number 840042 Phoenix Arizona 85016 —
Investigational Site Number 840056 Phoenix Arizona 85027 —
Investigational Site Number 840004 Tucson Arizona 85712 —
Investigational Site Number 840023 Covina California 91723 —
Investigational Site Number 840058 La Mesa California 91942 —
Investigational Site Number 840022 Santa Monica California 90904 —
Investigational Site Number 840050 Farmington Connecticut 06033 —
Investigational Site Number 840027 Stamford Connecticut 06905 —
Investigational Site Number 840051 Waterbury Connecticut 06708 —
Investigational Site Number 840011 Bradenton Florida 84020 —
Investigational Site Number 840036 Fort Lauderdale Florida 33316 —
Investigational Site Number 840017 Jupiter Florida 33458 —
Investigational Site Number 840038 New Port Richey Florida 34652 —
Investigational Site Number 840041 Pensacola Florida 32504 —
Investigational Site Number 840047 Sarasota Florida 34232 —
Investigational Site Number 840049 South Miami Florida 33134 —
Investigational Site Number 840039 Marietta Georgia 30060 —
Investigational Site Number 840005 Meridian Idaho 83642 —
Investigational Site Number 840002 Chicago Illinois 60611 —
Investigational Site Number 840043 Wichita Kansas 67203 —
Investigational Site Number 840012 Lexington Kentucky 40509 —
Investigational Site Number 840033 Traverse City Michigan 49648 —
Investigational Site Number 840037 St Louis Missouri 63128 —
Investigational Site Number 840007 Reno Nevada 89502 —
Investigational Site Number 840048 Egg Harbor New Jersey 08234 —
Investigational Site Number 840024 Amherst New York 14226 —
Investigational Site Number 840029 Hartsdale New York 10530 —
Investigational Site Number 840014 Rochester New York 14609 —
Investigational Site Number 840044 Asheville North Carolina 28801 —
Investigational Site Number 840028 Raleigh North Carolina 27612 —
Investigational Site Number 840045 Wilmington North Carolina 28401 —
Investigational Site Number 840046 Columbus Ohio 43213 —
Investigational Site Number 840013 Altoona Pennsylvania 16635 —
Investigational Site Number 840055 Philadelphia Pennsylvania 19107 —
Investigational Site Number 840018 Reading Pennsylvania 19611 —
Investigational Site Number 840026 Mt. Pleasant South Carolina 29464 —
Investigational Site Number 840052 Memphis Tennessee 38163 —
Investigational Site Number 840054 Austin Texas 78751 —
Investigational Site Number 840040 Bedford Texas 76021 —
Investigational Site Number 840010 Dallas Texas 75235 —
Investigational Site Number 840009 Draper Utah 84020 —
Investigational Site Number 840032 Salt Lake City Utah 84107 —
Investigational Site Number 840016 Charlottesville Virginia 22901 —
Investigational Site Number 840003 Seattle Washington 98166 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 3 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01618708, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jul 11, 2016 · Synced Oct 22, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01618708 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →