RECRUITING

Fibulink Syndesmosis Repair System With Early Full-Weight Bearing

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 purpose of the study is to evaluate the ability of the Fibulink Syndesmosis Repair System to maintain reduction of the ankle syndesmosis. Appropriate reduction of the syndesmosis is critical due the changes in tibiotalar contact pressure observed in cadaveric studies.6,7 Malreduction and instability of the distal tibiotalar joint can lead to chronic instability, increased articular damage and ultimately degenerative arthritis.7,8 Medial to lateral translation of distal tibia and fibula of 2 mm or more has been considered pathologic.9 Earlier biomechanical study demonstrated the Fibulink system is superior in maintaining displacement of less than 2 mm.4 Given the improved strength, we also look to evaluate the outcomes of initiating full weight bearing (100%) with Controlled Ankle Motion (CAM) boot at 4 weeks postoperatively. One of the big limitations for trans-osseous screw fixation is delayed weight bearing due to risk of screw breakage.1 Suture button technique allowed for early weight bearing with average of 6 weeks postoperatively using TightRope.2,10-12By initiating full weight bearing (100%) with CAM boot at 4 weeks postoperatively, this would be a significant improvement in current clinical practice.

Official Title

Evaluation of Safety and Performance Outcomes of the Fibulink Syndesmosis Repair System With Early Full-Weight Bearing

Quick Facts

Study Start:2023-07-13
Study Completion:2026-06-30
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06085586

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:22 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * ankle fracture with syndesmotic disruption as assessed with intra-operative cotton test.
  2. * Syndesmotic sprain (without fractures)
  3. * Bimalleolar equivalent ankle fractures
  4. * Bimalleolar ankle fractures
  5. * Maisonneuve fractures
  6. * Trimalleolar ankle fractures without the need for posterior malleolus fixation
  7. * Ankle fracture dislocations
  1. * 1) previous ankle surgery, 2) active local infection about the ankle, 3) chronic ankle deformity secondary to trauma or congenital, 4) ligamentous laxity, 5) pathologic fractures, 6) peripheral vascular disease, 7) peripheral neuropathy, 8) diabetes neuropathy and charcot, 9) open fractures, 10) poly trauma, 11) inability to provide informed consent, 12) symptomatic ankle osteoarthritis, 12) retained hardware, 13) pregnant, 14) metabolic bone disease, 15) history of chronic steroid use, 16) mal-reduced ankle fractures

Contacts and Locations

Study Contact

Amr A Abdelgawad, MD PhD MBA
CONTACT
7182837400
aabdelgawad@maimonidesmed.org
Ariel N Rodriguez, MD
CONTACT
7182837400
arrodriguez@maimonidesmed.org

Principal Investigator

Amr A Abdelgawad, MD PhD MBA
PRINCIPAL_INVESTIGATOR
Vice Chair of Orthopedic Clinical Programs, Director of Pediatric Orthopedic Surgery

Study Locations (Sites)

Maimonides Medical Center
Brooklyn, New York, 11219
United States

Collaborators and Investigators

Sponsor: Maimonides Medical Center

  • Amr A Abdelgawad, MD PhD MBA, PRINCIPAL_INVESTIGATOR, Vice Chair of Orthopedic Clinical Programs, Director of Pediatric Orthopedic Surgery

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 Date2023-07-13
Study Completion Date2026-06-30

Study Record Updates

Study Start Date2023-07-13
Study Completion Date2026-06-30

Terms related to this study

Keywords Provided by Researchers

  • Ankle Fractures
  • Bimalleolar Fractures
  • Bimalleolar Equivalent Fracture
  • Trimalleolar Fractures
  • Maisonneuve Fractures
  • Syndesmotic Injuries
  • Ankle Dislocations

Additional Relevant MeSH Terms

  • Ankle Fractures
  • Bimalleolar Fractures
  • Syndesmotic Injuries
  • Bimalleolar Equivalent Fracture
  • Maisonneuve Fracture
  • Trimalleolar Fractures
  • Ankle Dislocation