Design and Application of Nasal Stents (NCT05243147) | Clinical Trial Compass
CompletedNot Applicable
Design and Application of Nasal Stents
China80 participantsStarted 2020-10-22
Plain-language summary
Comparative study of nasal stents and nasal packing in patients undergoing septoplasty
Who can participate
Age range
18 Years – 70 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
. The subjects voluntarily participate in the experiment and sign the informed consent;
. Age range from 18 to 70 years old, gender unlimited;
. With nasal congestion as the chief complaint, CT of sinus suggested deviation of nasal septum with indications of surgery (deviation of nasal septum affects breathing and nasal congestion is serious; High nasal septum deviation affects sinus drainage or causes reflex headache; Nasal septum spine often causes nasal bleeding; Nasal septum deviation affects eustachian tube function);
. No history of respiratory tract infection and nasal decongestant use within 1 month before the visit;
. No other treatment was used;
. ASA grade 1\~2;
. Able to communicate well with researchers and follow the requirements of the experiment.
Exclusion criteria
. There are acute and chronic rhinosinusitis, nasal polyps, benign and malignant tumors and other nasal diseases;
. History of craniocerebral and nasal surgery;
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.
. The results of preoperative coagulation function test exceeded 20% of the upper limit of normal value;
. Patients known to be allergic to test instrument materials;
. Pregnant or lactating women;
. Other organoplastic or functional diseases complicated by the subjects limited their participation in the study and could not comply with the follow-up or affect the scientific integrity of the study;
. Participants who have participated in other clinical trials within the last 1 month;
. Participants considered unsuitable for this clinical trial for other reasons.