An observational study in Dupuytren's Contracture, sponsored by Endo Pharmaceuticals. Terminated at 7 sites in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2024-04-16.
Sponsored by Endo Pharmaceuticals (part of Keenova Therapeutics plc) · Observational
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.
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.
78 studies on the registry are indexed under Dupuytren Contracture; 18 are open to participants now.
This study's enrollment of 130 is above the median of 80 across 19 observational studies indexed under Dupuytren Contracture.
Browse Dupuytren Contracture studies →Endo Pharmaceuticals is the lead sponsor of 99 studies on the registry; none are open to participants now.
Of its 16 completed or terminated interventional studies of FDA-regulated products, 14 (88%) have results posted.
First submitted before Endo Pharmaceuticals became part of Keenova Therapeutics plc.
Counted across the registry records on this site, refreshed daily.
Participants with a confirmed diagnosis of DC will be enrolled in the United States.
Key Inclusion Criteria:
Key Exclusion criteria:
Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.
You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.
Informed consent
Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.
You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Number of Participants Receiving Each Treatment Type for DC
Time frame: Up to 36 months
Change from Baseline in Michigan Hand Questionnaire (MHQ) Scale Score
Time frame: Up to 36 months
Change from Baseline in European Quality of Life Five Dimension (EQ-5D) Questionnaire Score
Time frame: Up to 36 months
Change from Baseline in Unité Rhumatologique des Affections de la Main (URAM) Scale Score
Time frame: Up to 36 months
Participant Satisfaction Questionnaire
Time frame: Up to 36 months
Number of Participants Receiving Post-Procedural Care by the Treating Physician
Time frame: Up to 36 months
This study is terminated, as verified in Apr 2024. You cannot join it, but the record below documents what was studied.
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