BridgeMD
Tests treatment safety and results for Spinal Fusion
Official title Safety and Efficacy of Subdermal Betadine During Posterior Spinal Fusion
ClinicalTrials.gov ID: NCT06744907
What this study is testing
What is 10% Povidone-Iodine Arm?
10% Povidone-Iodine Arm is an investigational medicine, given as a treatment applied to the skin, being studied as a potential treatment for spinal fusion.
Plain-language explanation of the investigational treatment - it is being studied and is not an approved or proven therapy. The study team can confirm the details.
- What it's testing
- 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.
- Phase 4: studies an already-approved treatment
- Which group you join is decided by chance.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages up to 26
You may be able to join if
- Males and females
- Undergoing primary posterior spinal fusion of the thoracic and/or lumbar spine
- English Speaking
You likely can't join if
- Patients who have undergone prior spinal surgery
- Undergoing procedures other than primary posterior spinal fusion of the thoracic and/or lumbar spine (cervical fusion, anterior surgery...
- Any contraindication to povidone-iodine, including pregnancy, allergy, or prior treatment with radioiodine
The study team makes the final eligibility decision.
Where it's taking place
- Akron, Ohio, United States
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling all sexes, up to 26 years. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Akron, Ohio, United States. Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.