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Brief Title: Real-World Data Study to Understand Participant Treatment Outcomes for Dupuytren's Contracture
Official Title: Generating Real-world Ambispective Data to Study Participant Treatment Outcomes for Dupuytren's Contracture
Study ID: NCT05877066
Brief Summary: This is an observational study, meaning participants will not receive any investigational treatment as part of this study. Researchers will collect real-world data (RWD), based on usual care, to gain a more in-depth knowledge of the natural history and the treatment outcomes of Dupuytren's Contracture (DC) to evaluate the management of DC.
Detailed Description: Each participant of the study will have their data collected from the date of confirmed diagnosis of DC to the date of enrollment in the registry, post consent. Data will be collected from the participants clinical records as well as from the participant directly. Data will be collected through Pulse Infoframe's technology platform.
Minimum Age: 18 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
Endo Pharmaceuticals Clinical Site 6, Phoenix, Arizona, United States
Endo Pharmaceuticals Clinical Site 5, Greenwich, Connecticut, United States
Endo Pharmaceuticals Clinical Site 4, Temple Terrace, Florida, United States
Endo Pharmaceuticals Clinical Site 2, Indianapolis, Indiana, United States
Endo Pharmaceuticals Clinical Site 1, Eatontown, New Jersey, United States
Endo Pharmaceuticals Clinical Site 7, Charlotte, North Carolina, United States
Endo Pharmaceuticals Clinical Site 3, Bend, Oregon, United States
Name: Medical Information
Affiliation: Endo Pharmaceuticals
Role: STUDY_DIRECTOR