Cystic Fibrosis Clinical Trial
Official title:
Non-Invasive Ventilation (NIV) For Positive Pressure Support. A Randomised Cross-Over Trial To Evaluate The Short-Term Effects of NIV As An Adjunct To Airway Clearance Techniques in Adults With Cystic Fibrosis.
Cystic Fibrosis (CF) is a genetic disorder of altered ion transport across cell membranes
which is characterised by the production of thickened bodily secretions, affecting the
function of organs such as the pancreas and the lungs. Within the lungs, thickened sputum is
very difficult to clear, which can results in recurrent chest infections, which can lead to
lung damage. therefore it is important to optimise the removal of sputum to try and prevent
these complications. Traditionally, a variety of approaches are usually combined including
inhaled medications to thin or hydrate secretions, and chest physiotherapy to mobilise
secretions and improve sputum clearance.
There are many chest physiotherapy or airway clearance techniques (ACT) available including
breathing methods such as the Active Cycle of Breathing Techniques (ACBT) or Autogenic
Drainage (AD) and adjuncts such as Positive Expiratory Pressure (PEP), High Frequency Chest
Oscillation (the "Vest"), or oscillatory devices such as the Flutter or Acapella. When people
with CF have an infection or have severe disease often the effectiveness of ACTs can decrease
due to fatigue, shortness of breath or having an overwhelming amount of sputum. At this time
it is necessary to re-assess ACTs and the addition of positive pressure to airway clearance
techniques has been shown to be helpful in decreasing fatigue during chest physiotherapy.
At present no research studies have reported an increase in sputum cleared with the addition
of positive pressure, however it is thought that the ability to take a deeper breath when
using positive pressure would help to improve sputum clearance. With clinical experience of
the use of NIV with adult CF patients, the investigators aim to explore this objectively in
this study.
Research Question:
Does the addition of non-invasive ventilation (Breas, I-Sleep 25) as supplementary positive
pressure to normal airway clearance techniques improve sputum clearance in stable adult
patients with cystic fibrosis?
Hypothesis
The inclusion of non-invasive ventilation in addition to a patient's normal airway clearance
technique will lead to improvements in subjective ease of clearance and work of breathing
during airway clearance and objectively increase sputum clearance, as well as being well
tolerated in patients as an adjunct to airway clearance.
Cystic Fibrosis (CF) is a genetic disorder of altered ion transport across cell membranes
which is characterised by the production of thickened bodily secretions, affecting the
function of organs such as the pancreas and the lungs. Within the lungs, thickened mucus
alters normal mucocillary clearance mechanisms resulting in airway obstruction, mucus
plugging and recurrent infections. The cycle of recurrent infections and subsequent
inflammation is thought to be the major mechanism towards damage to lung tissue and the
occurrence of fibrosis, which decreases lung function, lowers tissue oxygenation and
eventually leads to respiratory failure and death. Optimisation of the removal of airway
secretions is therefore an integral part of the management of CF in order to try and prevent
these complications. Traditionally, a variety of approaches are usually combined including
mucolytic or hydrator therapy to make the secretions less viscous, and chest physiotherapy to
mobilise secretions and improve airway clearance.
There are many chest physiotherapy or airway clearance techniques (ACT) available including
breathing methods such as the Active Cycle of Breathing Techniques (ACBT) or Autogenic
Drainage (AD) and adjuncts such as Positive Expiratory Pressure (PEP), High Frequency Chest
Oscillation (the "Vest"), or oscillatory devices such as the Flutter or Acapella. Research
has shown there to be no difference in effectiveness between techniques, as long as they are
performed correctly and regularly, and therefore choice of ACT depends upon assessment of the
patient by a trained physiotherapist and discussions with the individual. With advancing
disease or infections, often the effectiveness of ACTs can decrease due to patient fatigue,
shortness of breath or overwhelming amount of secretions. At this time it is necessary to
re-assess ACTs, and the addition of positive pressure to airway clearance techniques has been
shown to decrease patient fatigue and respiratory rates during clearance. One of these
studies also demonstrated improvements in oxygenation and respiratory muscle strength after
the use of positive pressure with ACT. While no studies have reported an increase in sputum
expectorated with the addition of positive pressure, the ability to augment greater tidal
volumes through positive pressure is thought to be a mechanism which could improve sputum
clearance. Clinical experience at the Royal Brompton hospital has indicated that with
alterations in pressure and flow rates from resting settings, sputum clearance appears to be
easier and more effective; the investigators aim to explore this observation objectively in
this study.
Research Question:
Does the addition of non-invasive ventilation (Breas, I-Sleep 25) as supplementary positive
pressure to normal airway clearance techniques improve sputum clearance in stable adult
patients with cystic fibrosis?
Hypothesis
The inclusion of non-invasive ventilation in addition to a patient's normal airway clearance
technique will lead to improvements in subjective ease of clearance and work of breathing
during airway clearance and objectively increase sputum clearance, as well as being well
tolerated in patients as an adjunct to airway clearance.
;
| Status | Clinical Trial | Phase | |
|---|---|---|---|
| Completed |
NCT04696198 -
Thoracic Mobility in Cystic Fibrosis Care
|
N/A | |
| Completed |
NCT00803205 -
Study of Ataluren (PTC124™) in Cystic Fibrosis
|
Phase 3 | |
| Terminated |
NCT04921332 -
Bright Light Therapy for Depression Symptoms in Adults With Cystic Fibrosis (CF) and COPD
|
N/A | |
| Completed |
NCT03601637 -
Safety and Pharmacokinetic Study of Lumacaftor/Ivacaftor in Participants 1 to Less Than 2 Years of Age With Cystic Fibrosis, Homozygous for F508del
|
Phase 3 | |
| Terminated |
NCT02769637 -
Effect of Acid Blockade on Microbiota and Inflammation in Cystic Fibrosis (CF)
|
||
| Recruiting |
NCT06012084 -
The Development and Evaluation of iCF-PWR for Healthy Siblings of Individuals With Cystic Fibrosis
|
N/A | |
| Recruiting |
NCT06030206 -
Lung Transplant READY CF 2: A Multi-site RCT
|
N/A | |
| Recruiting |
NCT06032273 -
Lung Transplant READY CF 2: CARING CF Ancillary RCT
|
N/A | |
| Recruiting |
NCT05392855 -
Symptom Based Performance of Airway Clearance After Starting Highly Effective Modulators for Cystic Fibrosis (SPACE-CF)
|
N/A | |
| Recruiting |
NCT06088485 -
The Effect of Bone Mineral Density in Patients With Adult Cystic Fibrosis
|
||
| Recruiting |
NCT04039087 -
Sildenafil Exercise: Role of PDE5 Inhibition
|
Phase 2/Phase 3 | |
| Recruiting |
NCT04056702 -
Impact of Triple Combination CFTR Therapy on Sinus Disease.
|
||
| Completed |
NCT04058548 -
Clinical Utility of the 1-minute Sit to Stand Test as a Measure of Submaximal Exercise Tolerance in Patients With Cystic Fibrosis During Acute Pulmonary Exacerbation
|
N/A | |
| Completed |
NCT04038710 -
Clinical Outcomes of Triple Combination Therapy in Severe Cystic Fibrosis Disease.
|
||
| Completed |
NCT03637504 -
Feasibility of a Mobile Medication Plan Application in CF Patient Care
|
N/A | |
| Recruiting |
NCT03506061 -
Trikafta in Cystic Fibrosis Patients
|
Phase 2 | |
| Completed |
NCT03566550 -
Gut Imaging for Function & Transit in Cystic Fibrosis Study 1
|
||
| Recruiting |
NCT04828382 -
Prospective Study of Pregnancy in Women With Cystic Fibrosis
|
||
| Completed |
NCT04568980 -
Assessment of Contraceptive Safety and Effectiveness in Cystic Fibrosis
|
||
| Recruiting |
NCT04010253 -
Impact of Bronchial Drainage Technique by the Medical Device Simeox® on Respiratory Function and Symptoms in Adult Patients With Cystic Fibrosis
|
N/A |