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Spots Global Cancer Trial Database for Longterm Observational Study in Subjects Treated With AA4500 in AUX-CC-854, 856, 857, 858 & 859

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Trial Identification

Brief Title: Longterm Observational Study in Subjects Treated With AA4500 in AUX-CC-854, 856, 857, 858 & 859

Official Title: CORDLESS- Collagenase Optimal Reduction of Dupuytren's - Long-term Evaluation of Success Study

Study ID: NCT00954746

Interventions

Study Description

Brief Summary: The purpose of study AUX-CC-860 is to assess the durability of response of the AA4500 treatment regimen. This study will also evaluate long-term safety and progression of disease in joints.

Detailed Description: Phase 3 non-treatment study in which Year 2 to Year 5 year follow-up of subjects who received AA4500 in the 9-month open-label studies (AUX-CC-854 and AUX-CC-856) or the 12-month double-blind with open-label extension studies (AUX-CC-857/AUX-CC-858 and AUX-CC-859). After completion of one of the above mentioned studies, subjects are enrolled and followed once a calendar year for 4 consecutive years with at least 6 months between consecutive visits.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Hope Research Institute, Phoenix, Arizona, United States

Tucson Orthopedic Institute, P.C., Tucson, Arizona, United States

Providence Clinical Research, Burbank, California, United States

100 UCLA Medical Plaza, Suite 305, Los Angeles, California, United States

Hand Surgery Clinic, Palo Alto, California, United States

The Hand and Upper Extremity Center of Georgia, P.C., Atlanta, Georgia, United States

Southern Illinois Hand Center, S.C., Effingham, Illinois, United States

Rockford Orthopedic Associates, Ltd., Rockford, Illinois, United States

The Indiana Hand Center, Indianapolis, Indiana, United States

Via Christi Research, Wichita, Kansas, United States

Brigham and Women's Hospital, Department of Orthopedic Surgery, Boston, Massachusetts, United States

Newton-Wellesley Hospital, Newton, Massachusetts, United States

Marquette General Health System, Marquette, Michigan, United States

TRIA Orthopaedic Center, Minneapolis, Minnesota, United States

Hospital for Special Surgery, New York, New York, United States

SUNY Stony Brook - Department of Orthopedics, Stony Brook, New York, United States

The Bone and Joint Center, Bismark, North Dakota, United States

Health Research Institute, Oklahoma city, Oklahoma, United States

Hand Microsurgery & Reconstructive Orthopedics, Erie, Pennsylvania, United States

University Orthopedics Center, State College, Pennsylvania, United States

University Orthopedics, Inc., Providence, Rhode Island, United States

Alpha Clinical Research, Clarksville, Tennessee, United States

Accurate Clincal Research, Houston, Texas, United States

Royal North Shore Hospital, St Leonards, New South Wales, Australia

Rivercity Hospital, Auchenflower, Queensland, Australia

Caboolture Clinical Research Centre, Caboolture, Queensland, Australia

Peninsula Clinical Research, Kippa Ring, Queensland, Australia

Menzies Research Institute, Hobart, Tasmania, Australia

Emeritus Research, Malvern, Victoria, Australia

Gentofte Hospital, Hellerup, Copenhagen, Denmark

Hospital of Aalborg, Aalborg, , Denmark

Rigshospitalet, Copenhagen, , Denmark

Dextra, Helsinki, , Finland

Koskiklinikka, Tampere, , Finland

Department of Hand Surgery, Malmo, , Sweden

Department of Hand Surgery, Akademiska University Hospital, Uppsala, , Sweden

Pulvertaft Hand Clinic, Derby, Derbyshire, United Kingdom

Newcastle Biomedicine Clinical Research Facility, Newcastle, Newcastle Upon Tyne, United Kingdom

Welsh Centre for Plastic Surgery Morriston Hospital, Swansea, Wales, United Kingdom

Contact Details

Name: Veronica Urdaneta, MD

Affiliation: Endo Health Solutions

Role: STUDY_DIRECTOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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