Biomarkers for Predicting the Response to Inhaled Corticosteroid in Patients With Chronic Cough. (NCT05888350) | Clinical Trial Compass
CompletedNot Applicable
Biomarkers for Predicting the Response to Inhaled Corticosteroid in Patients With Chronic Cough.
China502 participantsStarted 2023-04-01
Plain-language summary
To investigate the value of blood eosinophils, FeNO and total IgE in predicting the response to inhaled corticosteroid in patients with chronic cough.
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
. Age: 18-70 years;
. Coughing lasting ≥ 8 weeks;
. No abnormality in chest imaging in the past 3 months (or there is abnormality but the investigator judges it not the cause of chronic cough);
. FEV1% pred\>70%;FEV1/FVC\>70%;
. VAS≥30 in the past 48 hours;
. Non-smokers or patients smoked less than 10 pack-years;
. Candidates voluntarily participate in and abide by the relevant regulations of the study, can cooperate with corresponding inspections, follow the follow-up plan, and voluntarily sign written informed consent.
Exclusion criteria
. Patients received inhaled or oral corticosteroids or leukotriene receptor antagonist in previous 4 weeks;
. Patients with history of upper respiratory tract infection in the past 8 weeks;
. Patients taking angiotensin-converting enzyme inhibitors in previous 8 weeks;
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.
What they're measuring
1
Cough VAS change from baseline to the 4th week
Timeframe: the 4th week
Trial details
NCT IDNCT05888350
SponsorThe First Affiliated Hospital of Guangzhou Medical University
. Female subjects who are pregnant, breast-feeding or risk of becoming pregnant during the study;
. Combined with a definite history of pulmonary diseases such as bronchiectasis, pulmonary interstitial disease, and pulmonary hypertension. Combined with other serious diseases (such as cardiovascular system diseases, metabolic system diseases, immune system diseases, nervous system diseases, etc.) that may affect the normal process of this study;
. Participating in other drug clinical trial projects.