Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT07347366

Electromagnetic High-Frequency Chest Wall Oscillation on Pulmonary Mucus Clearance in Patients With Impaired Self-Expectoration

Led by Pusan National University Yangsan Hospital · Updated on 2026-01-16

45

Participants Needed

1

Research Sites

66 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This exploratory study aims to evaluate the efficacy and safety of an electromagnetic high-frequency, low-strain chest wall oscillation device for enhancing pulm

CONDITIONS

Official Title

Electromagnetic High-Frequency Chest Wall Oscillation on Pulmonary Mucus Clearance in Patients With Impaired Self-Expectoration

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Hospitalized patients who require sputum clearance.
  • Patients with fever or respiratory symptoms (cough, sputum) and imaging findings indicating need for mucus clearance.
  • Adults aged 18 years or older who have signed informed consent or have consent from a legal representative.
Not Eligible

You will not qualify if you...

  • Patients with severe pneumonia needing ICU treatment.
  • Patients with major pulmonary diseases other than pneumonia, such as active tuberculosis or lung cancer.
  • Patients with severe respiratory failure (PaO2/FiO2 ≤ 200 mmHg).
  • Patients with unstable cardiovascular disease (recent myocardial infarction or NYHA class 3 or higher heart failure).
  • Patients hospitalized for head and neck trauma with unhealed surgical sites.
  • Patients with serious cardiac arrhythmias or hemodynamic instability.
  • Patients with recent pneumothorax or massive hemoptysis within 6 months, or current hemoptysis.
  • Patients with spinal surgery within 6 months or acute spinal injury.
  • Patients with osteoporosis.
  • Patients with bronchopleural fistula.
  • Pregnant or breastfeeding women.
  • Patients diagnosed with cervical disc disease.
  • Individuals who have participated in two or more clinical studies in the same year or another study within 6 months (except chronic lung disease cohort studies).
  • Patients with other clinically significant findings judged unsuitable by investigators.

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Rehab lab, Pusan National University Yangsan Hospital

Yangsan, Gyeongsangnam-do, South Korea, 50612

Actively Recruiting

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Research Team

J

Jisoo Baik, Doctoral

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

3

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