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โ† Trials
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Acapella vs Flutter Devices for Improving Breathing and Lung Function After Lobectomy

RecruitingNAAges 35 Years - 54 YearsAllRiphah International University
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In plain words

What the trial is, and whether it could suit you

Lobectomy patients frequently experience postoperative respiratory complications such as secretion retention, dyspnea, impaired gas exchange, and reduced lung function, which can delay recovery. Oscillatory Positive Expiratory Pressure (OPEP) devices such as Acapella and Flutter are commonly used to improve airway clearance and pulmonary function. This study aims to compare the effects of Acapella and Flutter devices on secretion clearance, dyspnea, arterial blood gases, and lung function in post-lobectomy patients.

Sign in to get the eligibility rules as simple questions to take to your doctor.

๐Ÿ“‹ Eligibility rules (as published)
Inclusion Criteria: * Patients aged 35 to 54 years * Both male and female patients * Patients who have undergone lobectomy surgery * Hemodynamically stable patients * Patients with adequate respiratory function (able to maintain oxygenation) * Patients 48 hours post-surgery * Patients who provide written informed consent to participate in the study Exclusion Criteria: * Hemodynamically unstable patients * Patients within less than 48 hours post-surgery * Presence of pneumothorax or air leak complications * Patients with recent major trauma or additional surgery * Patients with unstable cardiac conditions * Patients with massive hemoptysis * Patients unable to cooperate or perform breathing exercises with devices * Any contraindication to airway clearance techniques as judged by the clinician
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What it tests

  • Acapella Device Therapy (Experimental Arm 1):
  • Flutter Device Therapy (Experimental Arm 2):
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Where

1 site
Riphah International University
Lahore, Pakistan
๐Ÿค Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible โ€” always decide together with your own doctor.
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