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Real-World Data Study to Understand Participant Treatment Outcomes for Dupuytren's Contracture

NCT05877066 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 130

Last updated 2024-04-16

No results posted yet for this study

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.

Conditions

  • Dupuytren's Contracture

Sponsors & Collaborators

  • Pulse Infoframe

    collaborator INDUSTRY

  • Endo Pharmaceuticals

    lead INDUSTRY

Principal Investigators

  • Medical Information · Endo Pharmaceuticals

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-06-14
Primary Completion
2024-02-26
Completion
2024-02-26

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05877066 on ClinicalTrials.gov