Clinical Trials Directory

Trials / Recruiting

RecruitingNCT06840106

Nasal Steam Therapy for Post-extubation Respiratory Events

Effectiveness and Safety of Nasal Herbal Steam Therapy for Post-extubation Respiratory Events : Pragmatic Randomized Controlled, Parallel Grouped Study

Status
Recruiting
Phase
N/A
Study type
Interventional
Enrollment
66 (estimated)
Sponsor
Ilsan Cha hospital · Academic / Other
Sex
All
Age
19 Years – 69 Years
Healthy volunteers
Not accepted

Summary

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

Detailed description

This study aims to confirm the comparative effectiveness of nasal steam therapy by conducting a practical randomized controlled clinical trial comparing 66 patients complaining of upper respiratory symptoms with patients treated with a nasal steam therapy strategy (33 patients) and patients treated with a routine management strategy (33 patients). This study is a practical clinical study, and only randomly assigns patients to two groups: nasal steam therapy strategy and routine management strategy. The specific treatment method used is not determined in advance. The specific treatment is performed according to the clinical judgment according to the patient's condition. All treatment methods used during the study are recorded in the case report and compared. The treatment will be administered for a total of 5 days, and drug treatment may not be discontinued after the study period at the clinician's discretion.

Conditions

Interventions

TypeNameDescription
PROCEDURENasal steam therapyNasal 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
PROCEDURERoutine management strategyDepending 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.

Timeline

Start date
2025-02-18
Primary completion
2027-12-31
Completion
2027-12-31
First posted
2025-02-21
Last updated
2025-04-02

Locations

1 site across 1 country: South Korea

Source: ClinicalTrials.gov record NCT06840106. Inclusion in this directory is not an endorsement.