RECRUITING

Safety and Efficacy of Subdermal Betadine During Posterior Spinal Fusion

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

Bacterial in the subdermal layer of the skin, such as in hair follicles and sweat glands, may contaminate surgical wounds. The goal of this study is to learn about povidone-iodine and its ability to prevent infections specifically in patients with scoliosis receiving a spinal fusion.

Official Title

Subdermal Betadine to Reduce Microbacterial Bioburden During Posterior Spinal Fusion

Quick Facts

Study Start:2024-12-15
Study Completion:2026-11
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06744907

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:Not specified to 26 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:CHILD, 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

Alexandria Rundell, BS
CONTACT
330-543-3193
arundell@akronchildrens.org
Lorena Floccari, MD
CONTACT
330-543-3193
lfloccari@akronchildrens.org

Study Locations (Sites)

Akron Children's Hospital
Akron, Ohio, 44308
United States

Collaborators and Investigators

Sponsor: Akron Children's Hospital

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 Date2024-12-15
Study Completion Date2026-11

Study Record Updates

Study Start Date2024-12-15
Study Completion Date2026-11

Terms related to this study

Keywords Provided by Researchers

  • Spinal Fusion
  • Lumbar Spine
  • Thoracic Spine
  • Subdermal Betadine
  • Microbacterial bioburden

Additional Relevant MeSH Terms

  • Spinal Fusion