Proximal Phalanx Fractures Registry

Go Back to All Clinical Trials

Proximal Phalanx Fractures Registry

Brief description of study

The purpose of this study is to prospectively collect data and observe clinical outcomes following the treatment of proximal phalanx fractures with SOC modalities, including but not limited to closed reduction percutaneous pinning (CRPP), open reduction internal fixation (ORIF), and treatment with headless compression screws (HCS). Patients will be recruited and observed prospectively throughout the duration of their treatment. The approximate sample size will be 200 patients who present at NYU and related sites who have had a proximal phalanx fracture. Demographic data will be collected at initial visit and participants will be then be followed and observed longitudinally to determine the outcome of standard of care treatment options.

Clinical Study Identifier: s20-01751

Principal Investigator: Jacques H. Hacquebord.

Other Investigators: Omri B. Ayalon, Glenn A Teplitz, Steven Z. Glickel, Adam Jacoby, Jadie Elizabeth De Tolla, Nader Paksima, Ali Azad.

Contact the research team to learn more about this study.

Your Email

Not a valid e-mail address

Please Provide Email Address

First Name

First name is mandatory

Last Name

Your Phone

Please provide phone number

Invalid phone number

Valid phone number

Comments

Send Confirmation of This To Me

By clicking "Contact Research Team", your contact information will be sent securely to the research staff associated with the study. You will also receive a copy of this email in your inbox, as well as other notifications to determine your participation status in the study.

Clinical Research Studies