Respiration Disorders Clinical Trial
Official title:
Comparison Between the Manual Respiratory Exercises and Respiratory Pressure Meter
Pulmonary mechanics are further disturbed after cardiothoracic surgery that manifests like restrictive pathology, which may persist for weeks to months postoperatively. This experimental aimed to investigate the efficacy of a positive end-expiratory pressure device on maximum expiratory pressure, maximum voluntary ventilation, and dyspnea index in patients who underwent valve surgery.
Thirty male and female adolescent patients who underwent valve surgery aged 12-18 years old, recruited from the national heart institute enrolled in this experimental. They were assigned into two matched groups: Experimental group consisted of 15 patients, received positive end-expiratory pressure (PEEP) with a mouthpiece in addition to routine chest physiotherapy (postural drainage, percussion, vibration, and deep breathing exercises). Control group consisted of 15 patients, received routine chest physiotherapy alone. The program continued for four weeks. ;
Status | Clinical Trial | Phase | |
---|---|---|---|
Recruiting |
NCT03368612 -
Comparative Study Between the AirGoTM System and Standard Tests in the Assessment of the Respiratory Function
|
N/A | |
Recruiting |
NCT00530491 -
Prospective Trial to Reduce Morbidity and Mortality After Lung Surgery in Patients With Reduced Pulmonary Capacity
|
N/A | |
Active, not recruiting |
NCT04170348 -
Daily Vitamin D for Sickle-cell Respiratory Complications
|
Phase 2 | |
Recruiting |
NCT06019949 -
Spinal Cord Stimulation for Respiratory Rehabilitation in Patients With Chronic Spinal Cord Injury
|
N/A | |
Completed |
NCT05098808 -
Artificial Intelligence in Diagnosing Dysphagia Patients
|
||
Enrolling by invitation |
NCT01727518 -
The Austrian LEAD (Lung hEart sociAl boDy) Study
|
N/A | |
Recruiting |
NCT03709199 -
Long Term Follow up of Children Enrolled in the REDvent Study
|
||
Completed |
NCT01532180 -
Safety and Efficacy of a Hypoglossal Nerve Implant for the Treatment of Obstructive Sleep Apnea (OSA)
|
N/A | |
Completed |
NCT00750074 -
Slope of the Pressure-Time Waveform Predicts Resistance and Compliance in Mechanically Ventilated Subjects
|
N/A | |
Terminated |
NCT00464490 -
Use of Dexmedetomidine to Facilitate Extubation in Surgical ICU Patients Who Failed Previous Weaning Attempts
|
N/A | |
Completed |
NCT00202319 -
Effectiveness of Sedation Management in an Australian Intensive Care Unit
|
N/A | |
Completed |
NCT05270538 -
Cardiorespiratory and Acid-basic Imbalance Caused by Use of Mask
|
N/A | |
Terminated |
NCT02022072 -
Evaluation of Vital Capacity
|
Phase 2 | |
Recruiting |
NCT05398068 -
Effects of Exercise Training on Exercise Capacity and Sleep Quality in Patients With Obesity Hypoventilation Syndrome
|
N/A | |
Completed |
NCT03327610 -
Selecting the Best Ventilator Hyperinflation Settings
|
N/A | |
Completed |
NCT00665405 -
Atelectasis During Delivery - Comparing Cesarian (c) -Section and Labor
|
N/A | |
Completed |
NCT00004424 -
Randomized Study of Propofol Versus Fentanyl and Midazolam in Pediatric Patients Requiring Mechanical Ventilation and Sedation Therapy
|
N/A | |
Completed |
NCT04647383 -
A Study to Evaluate the Respiratory Safety of Lemborexant in Adult and Elderly Participants With Moderate to Severe Obstructive Sleep Apnea, and in Adult and Elderly Participants With Moderate to Severe Chronic Obstructive Pulmonary Disease
|
Phase 1 | |
Completed |
NCT01565954 -
Sleep Respiratory Disorders Evaluation in Sickle Cell Disease Children
|
||
Terminated |
NCT00394550 -
Treatment of Children With Obstructive Sleep Apnea and Laryngomalacia: the Role of Laser Supraglottoplasty
|
N/A |