RECRUITING

Quantitative and Clinical Assessment of Flexor Tendon Gliding Following Application of a Bioresorbable Hydrogel: A Prospective, Randomized Study in Patients Undergoing Distal Radius Fracture Repair

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

The investigators will be evaluating the use of versawrap in the setting of distal radius fractures by placing membrane between plate and flexor tendons. Investigators will then evaluate tendon gliding morphology and number of tendon ruptures

Official Title

Quantitative and Clinical Assessment of Flexor Tendon Gliding Following Application of a Bioresorbable Hydrogel: A Prospective, Randomized Study in Patients Undergoing Distal Radius Fracture Repair.

Quick Facts

Study Start:2021-09-13
Study Completion:2025-11
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT04976335

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Cognitively able to converse in English or in native language supported by a certified medical interpreter;
  2. * Diagnosed with a closed, distal radius fracture treated with open reduction and internal fixation using a volar distal radius plating system.
  1. * open injury;
  2. * concomitant injury to the contralateral wrist;
  3. * history of flexor tendon repair involving one or both hands or wrists;
  4. * use of a trans-carpal fixation device (bridge plate or external fixator) that would preclude wrist motion post-operatively;
  5. * concomitant fracture / injury to the thumb or index finger of one or both hands;
  6. * concomitant carpal tunnel release.

Contacts and Locations

Study Contact

Fraser J Leversedge, MD
CONTACT
919-316-0616
fraser.leversedge@cuanschutz.edu
Emma Judge
CONTACT
720-872-4850
emma.judge@cuanschutz.edu

Study Locations (Sites)

University of Colorado Health Hospital
Aurora, Colorado, 80045
United States
Denver Health Hospital
Denver, Colorado, 80204
United States

Collaborators and Investigators

Sponsor: University of Colorado, Denver

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2021-09-13
Study Completion Date2025-11

Study Record Updates

Study Start Date2021-09-13
Study Completion Date2025-11

Terms related to this study

Additional Relevant MeSH Terms

  • Distal Radius Fracture
  • Tendon Rupture