Nasal Steam Therapy for Post-extubation Respiratory Events
- Sponsor
- Ilsan Cha hospital
- Study ID
- NCT06840106
- Status
- Recruiting
Conditions
- Intubation
- Thyroid Cancer
Eligibility Criteria
- Sex
- ALL
- Age
- 19 Years - 69 Years
- Healthy Volunteers
- Not accepted
Interventions
- Nasal steam therapy — PROCEDURENasal steam therapy is performed once a every other day for a total of 3three times. The steam inhalation stimulates the acupoints of bilateral LI20, EX-HN8, and EX-HN9
- Routine management strategy — PROCEDUREDepending on the patient's symptoms and degree of improvement, the clinician may utilize all drugs currently used in clinical practice to improve upper respiratory symptoms, if necessary. All drugs that fall under the Anatomical Therapeutic Chemical Classification System (ATC) codes of non-disease treatment (R01), throat disease treatment (R02), lung disease or expectorant (R03, R05), and other respiratory organ drugs (R06, R07) and other drugs. The usage and dosage should be within the range of the current clinical guidelines.
Study Details
The effect of symptom improvement of nasal steam strategy compared to routine management strategy for upper respiratory symptoms occurring after endotracheal intubation in patients aged 19 years or older who underwent surgical removal under anesthesia requiring endotracheal intubation was evaluated by the difference in the results of Wisconsin Upper Respiratory Symptom Survey
Key Dates
- First listed
- Feb 21, 2025
- Start date
- Feb 18, 2025
- Status verified
- Mar 2025
- Primary completion
- Dec 31, 2027
- Completion
- Dec 31, 2027
Study Design
- Enrollment
- 66 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: Nasal Steam therapy strategyNasal steam therapy is performed once a every other day for a total of 3three times. The steam inhalation stimulates the acupoints of bilateral LI20, EX-HN8, and EX-HN9
- Active Comparator: Routine management strategyThis study is a practical clinical study, and the selection of drugs and other treatment methods will be based on the doctor's clinical judgment regarding the patient's symptoms, degree of improvement, etc. Drug administration or patient education will be implemented according to symptoms. Depending on the patient's symptoms and degree of improvement, the clinician may utilize all drugs currently used in clinical practice to improve upper respiratory symptoms, if necessary. All drugs that fall under the Anatomical Therapeutic Chemical Classification System (ATC) codes of non-disease treatment (R01), throat disease treatment (R02), lung disease or expectorant (R03, R05), and other respiratory organ drugs (R06, R07) and other drugs that clinicians orally administer in current clinical practice for the purpose of improving upper respiratory symptoms will be collected.
Primary Outcome Measure
Wisconsin upper respiratory symptom survey-24, WURSS-24 [ Time Frame: From enrollment to the end of treatment at Day 8, and follow up visit at Day 15 ]
Central Contacts
- Jee Young Lee, MD(KMD), PhD082-31-782-3113
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