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Not yet recruiting Not applicable NCT07536347

Effect of Adding PNF to IMT on Weaning Off MV

No applicable phase (e.g. observational)
Conditions: Weaning From Mechanical Ventilation

Sponsor: Beni-Suef University

trial.available_in: БГ
Overview
the goal of this clinical trial is to find out the effect of adding proprioceptive neuromuscular facilitation to inspiratory muscle training on weaning off mechanical ventilation. the main question it aims to answer is is there a significant difference in the effect of inspiratory muscle training combined with PNF on the duration of weaning in the mechanically ventilated ICU patients. researchers will compare effect of (Inspiratory muscle training combined with PNF) to (Inspiratory muscle training) and control group. participants will be mechanically ventilated both sexes patients will be recruited in this study from intensive care unit, their ages older than 18 years. The selected patients will be mechanically ventilated due to respiratory failure and will randomly assigned into three equal groups.
Description
type of study: randomized control trial this study is a prospective interventional study one that will be conducted on ninety three mechanically ventilated patients with respiratory failure of both sexes their ages older than 18 years from intensive care unit and will randomly assigned into three equal groups: 1. intervention group 1:include 31 mechanically ventilated patients will receive inspiratory muscle training along with Conventional rehabilitation program plus medical treatment. 2. intervention group 2: include 31 mechanically ventilated patients will receive inspiratory muscle training combined with proprioceptive neuromuscular facilitation along with Conventional rehabilitation program plus medical treatment. 3. Control group: include 31 mechanically ventilated patients will receive Conventional rehabilitation program plus medical treatment. Instrumentations: A) Evaluation: All the following will be measured for all patients who will participate in this study 1. ICU length of stay. 2. Monitoring: * Mode of ventilation parameters. * Fiao2 * PEEP * Tidal Volume * Respiratory Rate * The Duration and Type of Weaning: * Simple * Prolonged * Difficult * The patient vital signs: * Heart rate * Respiratory rate * Oxygen saturation 3. Maximum inspiratory pressure 4. Laboratory investigation: \- Arterial Blood Gases (ABG): for measurement of Pao2, Partial pressure of CO2 (Paco2), Hco3 and PH 5. Sonar parameters: \- Diaphragmatic excursion. 6. APHACH II score 7. Shallow breathing index. 8. Lung compliance: - Static and dynamic
Who can participate
Inclusion Criteria: * Adults of both sexes * patients older than 18 years * Conscious and cooperative * Hemodynamic stability without significant vasopressor support. * No continuous sedation. * Mechanically ventilated due to type 1 or type 2 respiratory failure (RF) for at least 24 hours. * Mechanically ventilated in assisted ventilation mode * Are able to participate in training actively, weanable as regard shallow breathing index. * presence of weaning criteria as defined in the European Consensus Conference in 2007, including sedation reduction, spontaneous breathing cycles, Partial pressure of oxygen (PaO2)/ fraction of inspired oxygen (FiO2) ≥ 150, absence of inotropes or vasopressors at high doses or increasing doses (\< 1 mg/h), oxy-hemoglobin saturation (SaO2) \> 90% with FiO2≤ 50%, positive end expiratory pressure (PEEP) ≤ 8 cmH2O, temperature between 36 and 39 °C. Exclusion Criteria: * Hemodynamic or respiratory instability * Condition that can compromise weaning, such as heart failure. * Condition that can prevent adequate performance of inspiratory muscle training, such as neuropathy or myopathy. * Thoracic or abdominal surgery precluding the use of PNF exercises * Rib fractures * Current pregnancy * Cardiac arrest with a guarded neurological prognosis * Deep coma
Interventions
threshold inspiratory muscle training + conventional chest physiotherapy
DEVICE
proprioceptive neuromuscular facilitation + threshold inspiratory muscle training + conventional chest physiotherapy
DEVICE
Conventional Chest Physiotherapy
OTHER
Locations

Location information is not available.

Technical details
Status
Not yet recruiting
Phase
Not applicable
Study type
INTERVENTIONAL
Sex
Male and female
Minimum age
18 Years
Healthy volunteers
No
Start date
25.04.2026
Completion date
01.12.2026
Registry ID
NCT07536347
Source
clinicaltrials.gov
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