Clinical trial · Observational
Real-World Data Study to Understand Participant Treatment Outcomes for Dupuytren's Contracture
Generating Real-world Ambispective Data to Study Participant Treatment Outcomes for Dupuytren's Contracture
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Why stopped (as posted): Endo determined to discontinue its registries and the GRASP registry enrollment has been closed.
Summary
Brief summary (as posted)
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
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Dupuytren's Contracture | Palmar Fibromatosis | ALIAS | 0.90 |
Interventions
Interventions (0)
Data not yet available
Design
Arms and outcomes
Arms (0)
[]Primary outcomes (1)
- measure
- Number of Participants Receiving Each Treatment Type for DC
- timeFrame
- Up to 36 months
Secondary outcomes (5)
- measure
- Change from Baseline in Michigan Hand Questionnaire (MHQ) Scale Score
- timeFrame
- Up to 36 months
- measure
- Change from Baseline in European Quality of Life Five Dimension (EQ-5D) Questionnaire Score
- timeFrame
- Up to 36 months
- measure
- Change from Baseline in Unité Rhumatologique des Affections de la Main (URAM) Scale Score
- timeFrame
- Up to 36 months
- measure
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Key Inclusion Criteria: * Any adult with a confirmed clinical diagnosis of DC. * Age 18 years (or age of majority in their jurisdiction) or older at time of enrollment. * Willing to participate in the registry (including completion of ePROs) and complete the informed consent form. * Having received DC treatment, either non-surgical or surgical, within 2 weeks before enrollment, at enrollment or any time after the date of enrollment or not having received DC treatment after confirmed diagnosis of DC. * Able to participate in English based registry. Key Exclusion criteria: * Not having a clinical diagnosis of DC. * Age less than 18 years. * Do not provide informed consent.
References
Publications (0)
Data not yet available