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Spots Global Cancer Trial Database for Real-World Data Study to Understand Participant Treatment Outcomes for Dupuytren's Contracture

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Trial Identification

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

Interventions

Study Description

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.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

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

Contact Details

Name: Medical Information

Affiliation: Endo Pharmaceuticals

Role: STUDY_DIRECTOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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