Diagnosis of Laryngeal Lesions Using the Probe-based Confocal Laser Endomicroscopy (NCT04139889) | Clinical Trial Compass
UnknownNot Applicable
Diagnosis of Laryngeal Lesions Using the Probe-based Confocal Laser Endomicroscopy
China60 participantsStarted 2017-06-01
Plain-language summary
To evaluate the diagnosis of laryngeal lesions using the Probe-based Confocal Laser Endomicroscopy in vivo.
Who can participate
Age range
18 Years – 85 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
. 18≤Male or female age ≤85 years old;
. patients with vocal cord lesions founded by white light laryngoscope and needed to perform laryngeal microsurgery;
. Willing and able to comply with study procedures and provide written informed consent to participate in the study.
Exclusion criteria
. Male or female \<18 years old, or Male or female \>85 years;
. The patient has abnormal blood or coagulation function, and there is a risk of bleeding during the examination;
. The patient has severe cardiopulmonary function or liver and kidney dysfunction and cannot tolerate surgery.
. The patient has a history of allergies to drugs or food.
. The patient has a positive serotonin sodium allergy test and is allergic to sodium fluorescein;
. Lactation or pregnant women.
. Refusal to sign the informed consent form.
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.