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

Primary Purpose

Cystic Fibrosis

Status
Terminated
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
Airways clearance and Hypertonic saline inhalation
Sponsored by
Belfast Health and Social Care Trust
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Cystic Fibrosis

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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.

    -

Sites / Locations

  • Belfast Health and Social Care Trust, Belfast City Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

ACTs after HTS inhalation:

ACTs during HTS inhalation

Arm Description

ACTs after HTS inhalation: Patients will take a bronchodilator (Salbutamol, 2 puffs) wait 15 minutes, and then take a single inhalation (4 mls) of 7% HTS (Nebusal™) via updraft nebulizer (Portex) (approximately 20 minutes) immediately followed by an airways clearance session of 10 supervised cycles of Active Cycle of Breathing Technique (ACBT) using the acapella® (approximately 20 minutes).

ACTs during HTS inhalation: Patients take a bronchodilator (Salbutamol, 2 puffs), wait 15 minutes, and then take a single inhalation (4mls) of 7% HTS (Nebusal™) through the acapella® duet (with portex updraft nebulizer attached) device. During inhalation, an airways clearance session of 10 supervised cycles of ACBT using the acapella® will be carried out (approximately 20 minutes).

Outcomes

Primary Outcome Measures

Lung Clearance Index

Secondary Outcome Measures

24 hour sputum volume

Full Information

First Posted
December 13, 2012
Last Updated
July 18, 2016
Sponsor
Belfast Health and Social Care Trust
Collaborators
Queen's University, Belfast, University of Ulster
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1. Study Identification

Unique Protocol Identification Number
NCT01753869
Brief Title
Timing of Hypertonic Saline Inhalation Relative to Airways Clearance in Cystic Fibrosis
Official Title
Timing of Hypertonic Saline Inhalation Relative to Airways Clearance in Cystic Fibrosis
Study Type
Interventional

2. Study Status

Record Verification Date
July 2016
Overall Recruitment Status
Terminated
Why Stopped
Challenges with recruitment
Study Start Date
December 2012 (undefined)
Primary Completion Date
June 2016 (Actual)
Study Completion Date
June 2016 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Belfast Health and Social Care Trust
Collaborators
Queen's University, Belfast, University of Ulster

4. Oversight

Data Monitoring Committee
No

5. Study Description

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)

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cystic Fibrosis

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
14 (Actual)

8. Arms, Groups, and Interventions

Arm Title
ACTs after HTS inhalation:
Arm Type
Active Comparator
Arm Description
ACTs after HTS inhalation: Patients will take a bronchodilator (Salbutamol, 2 puffs) wait 15 minutes, and then take a single inhalation (4 mls) of 7% HTS (Nebusal™) via updraft nebulizer (Portex) (approximately 20 minutes) immediately followed by an airways clearance session of 10 supervised cycles of Active Cycle of Breathing Technique (ACBT) using the acapella® (approximately 20 minutes).
Arm Title
ACTs during HTS inhalation
Arm Type
Active Comparator
Arm Description
ACTs during HTS inhalation: Patients take a bronchodilator (Salbutamol, 2 puffs), wait 15 minutes, and then take a single inhalation (4mls) of 7% HTS (Nebusal™) through the acapella® duet (with portex updraft nebulizer attached) device. During inhalation, an airways clearance session of 10 supervised cycles of ACBT using the acapella® will be carried out (approximately 20 minutes).
Intervention Type
Procedure
Intervention Name(s)
Airways clearance and Hypertonic saline inhalation
Primary Outcome Measure Information:
Title
Lung Clearance Index
Time Frame
90 minutes post treatment
Secondary Outcome Measure Information:
Title
24 hour sputum volume
Time Frame
24 hours post treatment
Other Pre-specified Outcome Measures:
Title
spirometry (FEV1% predicted; FEF25-75% [Forced expiratory flow 25-75] predicted)
Time Frame
90 minutes post treatment

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Male or female patients with a documented diagnosis of CF aged ≥18 years. Written informed consent. At least day 10 - 14 of IV antibiotic therapy during a hospital admission for a pulmonary exacerbation. Patients must be able to perform acceptable spirometric manoeuvres, according to the American Thoracic Society/ERS (ATS/ERS) standards (Miller, Hankinson et. al. 2005). Patient with an FEV1% predicted of ≥ 40%predicted (Stanojevic, Wade et al. 2008). Patients who are productive of sputum from screening visit to study visit 1 (≥10g over 24 hours). Patients who have been prescribed HTS (Nebusal 7%) and have successfully completed a challenge test. 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: Day 1-9 of IV antibiotic therapy during a hospital admission. Patients who are colonized with Burkholderia cepacia complex. Patient who are HTS naive. Patients who have an intolerance to HTS. Patients who are currently participating in another study or have participated in another study with an investigational drug within one month of screening. 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. -
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Judy M Bradley, PhD
Organizational Affiliation
University of Ulster
Official's Role
Principal Investigator
Facility Information:
Facility Name
Belfast Health and Social Care Trust, Belfast City Hospital
City
Belfast
ZIP/Postal Code
BT9 7JL
Country
United Kingdom

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
32352564
Citation
Morrison L, Milroy S. Oscillating devices for airway clearance in people with cystic fibrosis. Cochrane Database Syst Rev. 2020 Apr 30;4(4):CD006842. doi: 10.1002/14651858.CD006842.pub5.
Results Reference
derived
PubMed Identifier
28123751
Citation
O'Neill K, Moran F, Tunney MM, Elborn JS, Bradbury I, Downey DG, Rendall J, Bradley JM. Timing of hypertonic saline and airway clearance techniques in adults with cystic fibrosis during pulmonary exacerbation: pilot data from a randomised crossover study. BMJ Open Respir Res. 2017 Jan 12;4(1):e000168. doi: 10.1136/bmjresp-2016-000168. eCollection 2017.
Results Reference
derived

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

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