RECRUITING

Antibiotic Cement Bead Pouch Versus Negative Pressure Wound Therapy

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 Beads vs Vac trial is a multi-centre randomized controlled trial of 312 participants with a severe open tibia fracture requiring multiple irrigation and debridement surgeries. Eligible participants will be randomized to receive either an antibiotic bead pouch or negative pressure wound therapy (NPWT) for their temporary open fracture wound management. Outcomes will be assessed at 6 weeks, 3 months, and 6 months post-surgery. The primary outcome will be a composite outcome to evaluate clinical status six months after randomization. Components of the composite outcome will be hierarchically assessed in the following order: 1) all-cause mortality, 2) injury-related amputation of the lower extremity, 3) unplanned reoperation to manage wound complications, infection, or delayed fracture healing, and 4) clinical fracture healing as assessed using the Functional IndeX for Trauma (FIX-IT) instrument. The secondary outcomes will independently assess the four components of the primary outcome. This is a Phase III trial.

Official Title

A Randomized Controlled Trial Comparing Antibiotic Cement Bead Pouch Versus Negative Pressure Wound Therapy for the Management of Severe Open Tibia Fracture Wounds

Quick Facts

Study Start:2023-11-05
Study Completion:2025-10-01
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT05615844

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. Age 18 years or older
  2. Willing and able to provide informed consent
  3. Able to understand and follow study procedures
  4. Stable medical condition
  1. Pregnancy or breastfeeding
  2. Severe psychiatric disorders
  3. Active substance abuse
  4. Unstable medical conditions
  5. Inability to comply with study requirements

Contacts and Locations

Study Contact

Heather Phipps, MPS
CONTACT
410-706-2492
hphipps@som.umaryland.edu

Study Locations (Sites)

University of Southern California
Los Angeles, California, 90033
United States
University of Florida
Gainesville, Florida, 32611
United States
University of Miami
Miami, Florida, 33146
United States
Indiana University
Indianapolis, Indiana, 46202
United States
University of Maryland, R Adams Cowley Shock Trauma Center
Baltimore, Maryland, 21201
United States
University of Maryland Capital Region Health
Largo, Maryland, 20774
United States
University of Mississippi
University, Mississippi, 38677
United States
Bryan Medical Center
Lincoln, Nebraska, 68506
United States
Dartmouth-Hitchcock Medical Center
Lebanon, New Hampshire, 03766
United States
University of Cincinnati
Cincinnati, Ohio, 45219
United States
Bon Secours Mercy Health
Cincinnati, Ohio, 45237
United States
Ortegon Health & Science University
Portland, Oregon, 97239
United States
Prisma Health
Greenville, South Carolina, 29605
United States
University of Utah
Salt Lake City, Utah, 84112
United States
Inova Fairfax
Falls Church, Virginia, 22042
United States
University of Wisconsin
Madison, Wisconsin, 53792
United States

Collaborators and Investigators

Sponsor: University of Maryland, Baltimore

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 Date2023-11-05
Study Completion Date2025-10-01

Study Record Updates

Study Start Date2023-11-05
Study Completion Date2025-10-01

Terms related to this study

Additional Relevant MeSH Terms

  • Open Tíbia Fracture