Dyspnea During Activity

2

Review clinical trials related to Dyspnea During Activity. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Effect of Ipratropium Bromide on EILO

The investigators propose a study that compares breathlessness and airway obstruction during intense exercise in 34 children and adolescents with Exercise-Induced Laryngeal Obstruction after breathing in ipratropium bromide or placebo. It is hypothesized that breathlessness and airway obstruction will be lower following breathing in ipratropium bromide compared with placebo.

Participants needed: 50
Trial details
Phase: Phase 2Age: 8-17Biological sex: AllType: InterventionalSponsor: Cook Children's Health Care SystemUpdated: May 5, 2026Locations: 1
Eligibility criteria

Patients must be diagnosed with EILO confirmed by Continuous Laryngoscopy During... [+3]

Patients that do not have EILO. [+7]

Status: Recruiting

SWEEP: Shuttle Walking Test for Exercise Evaluation in Pulmonary Resection

This is a prospective observational study that evaluates whether the Shuttle Walking Test (SWT) can predict postoperative symptoms, particularly dyspnea, in patients with chronic respiratory diseases undergoing lung resection. Currently, tools such as DLCO or cardiopulmonary exercise testing (CPET) are used to assess surgical risk and exercise capacity before lung surgery. However, these tests are not always accessible due to equipment limitations or long waiting times. The SWT is a simpler, safer, and more cost-effective alternative that has been recently recognized as a new medical technology in Korea for evaluating exercise capacity. In this study, patients with chronic lung diseases (such as COPD, ILD, or bronchiectasis) who are scheduled to undergo lung resection will perform the SWT before surgery. Their symptoms and quality of life will be assessed through questionnaires before and three months after the surgery. The goal is to determine whether SWT results can help predict postoperative dyspnea and provide useful information for preoperative risk stratification.

Participants needed: 100
Trial details
Age: 40+Biological sex: AllType: ObservationalSponsor: Seoul National University Bundang HospitalUpdated: Aug 4, 2025Locations: 1Duration: 3 Months
Eligibility criteria

- Age ≥ 40 years [+4]

- Illiteracy or inability to read study materials [+3]