Clinical trial · Observational
CORRECT: COmmunity RegistRy Study Evaluating Dupuytren's Contracture Treatment
Community Registry Study Evaluating Dupuytren's Contracture Treatment. A Prospective, Observational, Longitudinal, Multicenter Study of the Treatment Patterns and Outcomes in Patients With Dupuytren's Contracture.
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
This observational study will prospectively collect data on treatment options, patient/investigator satisfaction, requirement for retreatment or additional treatment, and long-term outcomes of 3 treatment modalities(XIAFLEX, fasciectomy, or fasciotomy/needle aponeurotomy) in patients with Dupuytren's contracture. In addition, this study will provide additional health economics and utilization data.
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
- The primary objective is to collect real-world data regarding patient reported outcomes of the 3 primary treatment modalities in patients with Dupuytren's contracture.
- timeFrame
- 4 years
Secondary outcomes (1)
- measure
- Examine safety, effectiveness and association between treatments and selected healthcare utilization and patient report outcomes.
- timeFrame
- 4 years
- description
- The secondary objectives are as follows: * Examine the safety trends of various treatment options in patients with Dupuytren's contracture * Examine the effectiveness trends of various treatment options, specifically evaluating long term contracture recurrence * Examine the association between various treatment regimens and healthcare resource utilization * Examine the association between various treatments and patient-reported outcomes (PROs) such as disease burden, ADLs, hand functionality, work performance, time to return to work, treatment satisfaction, and patient preference
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: * Women or men 18 years of age or older * Patients with a Dupuytren's contracture of at least a single joint and a desire for correction * Patients who are able to read and understand English * Patients who are capable of understanding and cooperating with the requirements of the study * Patients who are willing and able to respond to the posttreatment assessments via telephone or internet * Patients must provide written informed consent, indicating that they understand the purpose of and requirements of the study and are willing to participate in the study. Exclusion Criteria: * Patients who decide not to pursue correction of the Dupuytren's contracture.
References
Publications (0)
Data not yet available