NCT06330545 · Dartmouth-Hitchcock Medical Center
Radiation Therapy for Dupuytren's Contracture Following Non-Surgical Release
What this study is about
The goal of this study is to learn about preventing recurrence of Dupuytren's Contracture. The main question it aims to answer are: • Does targeted radiation therapy decrease recurrence of Dupuytren's contracture after treatment with Collagenase Clostridium Histolyticum? Participants will undergo: * Release of Dupuytren's Contracture after Collagenase Clostridium Histolyticum injection * Daily radiation therapy treatment for 5 days followed by 6-8 week rest period and then another course of 5 days of radiation therapy
View original scientific description
The goal of this study is to learn about preventing recurrence of Dupuytren's Contracture.
Who can participate
This study lists these criteria on ClinicalTrials.gov. A study coordinator reviews eligibility during screening — this page does not determine whether you qualify.
Inclusion criteria
- Age 45 or greater with DC
- Extension deficit \>10 degrees
- Unable to simultaneously place the affected finger and palm flat on a table.
- Women included in the study will be post-menopausal or using contraception, and a pregnancy test will be performed as standard of care.
- For patients who are having multiple CCH injections, only the first 2 joints on given hand will be included
Exclusion criteria
- Unsuccessful non-surgical release (\> N/1 disease)
- They develop an open wound during CCH
- Breast feeding or pregnancy
- A chronic muscular, neurologic, or neuromuscular disorder affecting the hands.
- Less than the age of 45
- They have previously undergone radiation on the hand in which they plan to get CCH injections
- They are pregnant women, impaired adults or prisoners
Where
- Lebanon, New Hampshire
Frequently asked questions
What is a clinical trial?
A clinical trial is a research study that tests new medical treatments, drugs, devices, or procedures to determine their safety and effectiveness. Trials are carefully designed and monitored to protect participants while advancing medical knowledge.
Is it safe to participate?
Clinical trials follow strict safety guidelines and ethical standards. Trials must be reviewed and approved, and participants are closely monitored by medical professionals throughout the study. You can withdraw at any time if you choose.
Will I be compensated?
Many clinical trials offer compensation for your time, travel expenses, and inconvenience. The specific compensation varies by study and will be discussed during the screening process. All study-related medical care is typically provided at no cost to participants.
Will I receive a placebo instead of treatment?
When effective treatment exists, participants typically receive either the standard treatment plus the study intervention, or the standard treatment plus placebo. You would not be denied effective care. Placebos are primarily used when no proven treatment is available, or in addition to standard care. Your trial consent form will clearly explain what treatments you may receive.
Can I leave a trial if I change my mind?
Absolutely. Participation in clinical trials is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty or loss of benefits to which you are otherwise entitled.
How long does a clinical trial last?
Trial duration varies widely depending on the study design and purpose. Some trials last just a few weeks, while others may continue for months or years. The study coordinator will provide specific timeline information during your screening call.
Data: ClinicalTrials.gov · synced Nov 22, 2024 · Source of record for eligibility and locations