Evaluation of Neuroma Perfusion with Indocyanine Green Fluorescence Angiography (NCT06164392) | Clinical Trial Compass
WithdrawnPhase 4
Evaluation of Neuroma Perfusion with Indocyanine Green Fluorescence Angiography
Stopped: The attendings who were to participate did not want to alter their standard neuroma treatment of neurotomy and TMR, as opposed to dissecting the end of all neuromas before neurotomy. No patients were enrolled in the study.
United States0Started 2024-12-28
Plain-language summary
The purpose of this study is to characterize the perfusion of neuromas using indocyanine green fluorescence angiography
Who can participate
Age range
18 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Age \> 18 years
* Clinical diagnosis of neuroma
* Scheduled elective surgery for neuroma excision
Exclusion Criteria:
* Minors, or age \< 18 years old at the time of surgery
* Unable to provide written, informed consent
* Prisoners and decision-impaired individuals
* Pregnant or lactating women
* History of allergy to indocyanine green
* History of allergy to iodides
* History of allergic asthma
* History of hepatic failure
* History of renal failure
* Patients in whom the planned surgical incision/approach does not include excision of the neuroma
* Patients in whom adequate surgical exposure of the neuroma is unable to be obtained, as determined intraoperatively at the time of surgery by the Investigator or Co-Investigators
* Any subject who, at the discretion of the Investigator or Co-Investigators, is not suitable for inclusion in the study
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.