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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 Jul 22, 2026, 11:56 PM 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

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

  • Synvisc-One (hylan G-F 20) Device
  • Placebo Device

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
Aug 31, 2012
Primary completion
May 31, 2015
Completion
May 31, 2015
Last update posted
Jul 10, 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 10, 2016 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01618708 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →