Cystic Fibrosis
Conditions
Brief summary
Lung disease is the predominant cause of morbidity and mortality in Cystic Fibrosis (CF) with 80% of deaths resulting directly or indirectly from pulmonary disease. Abnormal airway clearance causes retention of mucus resulting in frequent chest infections. Physiotherapists use different techniques to help clear mucus from the lungs of patients with CF. Inhaled medications and airways clearance techniques (ACTs) are central to a CF patient's daily treatment and are often coordinated. Burden of treatment is a common reason for non-adherence in this patient group, and streamlining of treatment timings is sought to optimize adherence whilst ensuring efficacy to an often complex daily regimen of inhaled bronchodilators, nebulizers and ACTs. A gap in the research exists as to the optimal timing of Hypertonic Saline (HTS) and ACT within the daily regimen. A study to show whether the timing of HTS around ACT is significant, can better inform patients and potentially allow more flexibility around their treatment regimen. Lung Clearance Index (LCI) has shown good sensitivity to abnormalities in lung function compared with spirometry and has demonstrated a treatment effect in other trials. LCI may be a suitable tool therefore, to assess intervention strategies aimed at airways clearance in CF. This study aims to compare the effects ACTs after HTS inhalation versus ACTs during HTS inhalation as measured by LCI. It is a randomized, crossover trial of ACTs after HTS inhalation compared with ACTs during HTS inhalation in adult CF patients during day 10-14 of a hospital admission for treatment of a pulmonary exacerbation. Patients will be randomized to receive 1 of the treatment session options on the first day and the reverse on the second day. The primary objective of this study is to compare the change in LCI (a measure of lung function) at 90 minutes post treatment with ACTs after HTS inhalation compared with ACTs during HTS inhalation in adult CF patients. LCI (lung clearance index) ACT (airway clearance technique) HTS (hypertonic saline)
Interventions
PROCEDUREAirways clearance and Hypertonic saline inhalation
Sponsors
Queen's University, Belfast
University of Ulster
Belfast Health and Social Care Trust
Study design
Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
1. Male or female patients with a documented diagnosis of CF aged ≥18 years. 2. Written informed consent. 3. At least day 10 - 14 of IV antibiotic therapy during a hospital admission for a pulmonary exacerbation. 4. Patients must be able to perform acceptable spirometric manoeuvres, according to the American Thoracic Society/ERS (ATS/ERS) standards (Miller, Hankinson et. al. 2005). 5. Patient with an FEV1% predicted of ≥ 40%predicted (Stanojevic, Wade et al. 2008). 6. Patients who are productive of sputum from screening visit to study visit 1 (≥10g over 24 hours). 7. Patients who have been prescribed HTS (Nebusal 7%) and have successfully completed a challenge test. 8. Any other chronic medication must have commenced therapy 4 weeks prior to screening and be willing to continue this therapy for the entire duration of the study.
Exclusion criteria
1. Day 1-9 of IV antibiotic therapy during a hospital admission. 2. Patients who are colonized with Burkholderia cepacia complex. 3. Patient who are HTS naive. 4. Patients who have an intolerance to HTS. 5. Patients who are currently participating in another study or have participated in another study with an investigational drug within one month of screening. 6. Clinically significant disease or medical condition other than CF or CF-related conditions that, in the opinion of the Investigator, would compromise the safety of the patient or the quality of the data. \-
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Lung Clearance Index | 90 minutes post treatment |
Secondary
| Measure | Time frame |
|---|---|
| 24 hour sputum volume | 24 hours post treatment |
Other
| Measure | Time frame |
|---|---|
| spirometry (FEV1% predicted; FEF25-75% [Forced expiratory flow 25-75] predicted) | 90 minutes post treatment |
Countries
United Kingdom
Outcome results
None listed