Timing of Hypertonic Saline Inhalation Relative to Airways Clearance in Cystic Fibrosis

Cystic Fibrosis Clinical Trial

Official title:

Timing of Hypertonic Saline Inhalation Relative to Airways Clearance in Cystic Fibrosis

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT01753869
• Other study ID #: 12025JB-AS
• Status: Terminated
• Phase: N/A
• First received: December 13, 2012
• Last updated: July 18, 2016
• Start date: December 2012
• Est. completion date: June 2016

Study information

• Verified date: July 2016
• Source: Belfast Health and Social Care Trust
• Contact: n/a
• Is FDA regulated: No
• Health authority: United Kingdom: Research Ethics Committee
• Study type: Interventional

Clinical Trial 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)

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 14
• Est. completion date: June 2016
• Est. primary completion date: June 2016
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years and older

Eligibility

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.

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Crossover Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Treatment

Related Conditions & MeSH terms

• Cystic Fibrosis
• Fibrosis

Intervention

Procedure:
• Airways clearance and Hypertonic saline inhalation

Locations

Country	Name	City	State
United Kingdom	Belfast Health and Social Care Trust, Belfast City Hospital	Belfast

Sponsors (3)

Lead Sponsor	Collaborator
Belfast Health and Social Care Trust	Queen's University, Belfast, University of Ulster

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	spirometry (FEV1% predicted; FEF25-75% [Forced expiratory flow 25-75] predicted)		90 minutes post treatment	No
Primary	Lung Clearance Index		90 minutes post treatment	No
Secondary	24 hour sputum volume		24 hours post treatment	No