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Cystic FibrosisNCT03261219

IPV vs CPT for Airway Clearance During CF Exacerbation

A study testing Intrapulmonary Percussive ventilation and Chest Physiotherapy Vest (Incourage) in people with Cystic Fibrosis and Airway Clearance Impairment, run by University of Florida.

Withdrawn

Withdrawn. The study stopped before anyone enrolled.

Official record
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Trial summary

Intrapulmonary Percussive Ventilation (IPV) will show greater improvements in Forced Expiatory Volume in 1 second (FEV1) shorter duration of stay, and greater time to next pulmonary exacerbation in pediatric Cystic Fibrosis patients admitted for pulmonary exacerbation. Read more about this study

Who is it for?
Ages 5 to 21 years
Conditions the study is for
Cystic Fibrosis, Airway Clearance Impairment
What is being tested?
Intrapulmonary Percussive ventilation and Chest Physiotherapy Vest (Incourage)
Type of treatment
Medical device
Could I receive a placebo?
No, everyone receives an active treatment
How many people
0 participants
Where
No sites listed yet
Study dates
Jul 2018to 30 Oct 2018
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 5 to 21 years
  • All sexes
  • No healthy volunteers
  • Child, Adult

Who may be able to join

  • CF patient admitted for pulmonary exacerbation

Who cannot join

  • Patients who are not able to perform spirometry, patients with neurological impairment (Cerebral Palsy) or severe behavioral problems that precludes consistent use of IPV, patients with pneumothorax or significant hemoptysis, patients who require supplemental oxygen or ventilatory support, or patients whose parents/guardians are not willing to consent will be excluded.

About this study

Official title: Intrapulmonary Percussive Ventilation vs Chest Physiotherapy Vest in Airway Clearance During Cystic Fibrosis Pulmonary Exacerbation

Intrapulmonary Percussive Ventilation (IPV) will show greater improvements in Forced Expiatory Volume in 1 second (FEV1) shorter duration of stay, and greater time to next pulmonary exacerbation in pediatric Cystic Fibrosis patients admitted for pulmonary exacerbation.

FEV1 is a measurement of obstruction in the airway which is seen to be elevated in CF patients with worsening lung disease. FEV1 is used as a primary endpoint in pulmonary trials because it is an acute indicator of worsening or improving lung function.

Read the detailed description

The study will be a prospective randomized clinical trial. All Cystic Fibrosis (CF) patients five years and above who are being admitted to University of Florida (UF) Shands Children's Hospital with the diagnosis of CF acute pulmonary exacerbations will be approached for study consent on day one of hospitalization.

Each patient will be randomized to receive either IPV (metaneb) or Chest Physiotherapy (CPT) vest (Incourage) therapy. Treatments will be administered by in-house respiratory therapists four times daily according to standard protocol, and the respiratory therapist will document each treatment in the patient's electronic medical record (EPIC). Each patient will also receive mucolytic agents (dornase alpha, hypertonic saline) and antibiotic therapy as per routine inpatient protocol per the attending pulmonologist on service. If the patient's clinical status worsens during their admission the attending pulmonologist will be allowed to change the airway clearance regimen or antibiotic coverage at their discretion.

If a patient is enrolled and has another admission for pulmonary exacerbation after their initial admission, we will attempt to randomize them to the other arm and utilize this data to see if there is a difference in outcome parameters for the same patient if they are randomized to both arms.

The degree of improvement in FEV1 defined as absolute difference between admission FEV1 and discharge FEV1 will be used as primary outcome measure to compare effectiveness between both modalities. This measure is commonly used in the Cystic Fibrosis community of clinicians and researchers as measure of airway obstruction and disease severity. We will perform spirometry at least twice, at admission and discharge, on these patients. The patient's spirometry from their office visit on the same day of admission or first spirometry during their admission will count as the initial spirometry. Last spirometry obtained before discharge will be the discharge spirometry. Additional spirometry may be performed during the patient's admission at the attending provider's clinical discretion. We will also use data from these additional spirometry measurements if they take place.

There will be no additional cost incurred by using the IPV device as opposed to standard of care (CPT vest).There is also no increased effort performing IPV treatments from the respiratory therapist performing the treatment or from the patient.

Length of hospital stay in days will be used as a secondary outcome.

Another secondary outcome measure will be the length of time between discharge and subsequent admissions for CF pulmonary exacerbation. We will follow the subject for an additional 6 months after they are enrolled to ascertain the time to next admission and total number of admissions in that time.

Other information that will be accessed through EPIC records will be number of admissions for CF pulmonary exacerbations, airway clearance regimen, radiological data, laboratory results (respiratory cultures, Respiratory Viral Panels, Acid Fast Bacilli cultures, complete Blood counts), vital signs, weight measurements, Bronchoscopy reports, medications used (Orkambi, Kalydeco, antibiotics), and oxygen requirement. All of this information will be collected in the time period of 1 year before study and throughout study,

We will also administer a 2 question questionnaire at the beginning and end of admission to the hospital in order to evaluate the patient/family opinion of the therapy they received during their participation in the study.

Being tested
Intrapulmonary Percussive ventilation, Chest Physiotherapy Vest (Incourage)
Medical subject headings
Cystic Fibrosis

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Intrapulmonary Percussive ventilationDevice

    mode of airway clearance using mouthpiece and alternating air currents applied directly to the airway

  • Chest Physiotherapy Vest (Incourage)Device

    mode of airway clearance using external vibratory vest

Study groups in NCT03261219
Study groupRoleWhat they receive
Intrapulmonary Percussive ventilationExperimentalNot described
Receives: Device: Intrapulmonary Percussive ventilation
Chest Physiotherapy vestActive comparatorNot described
Receives: Device: Chest Physiotherapy Vest (Incourage)

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. FEV1 change

    change in FEV1 from baseline at admission

    Measured: duration of hospital stay (usually 10-14 days)

Secondary outcomes (3)
  1. time to next admission

    time in days to next hospital admission for CF Pulmonary Exacerbation

    Measured: from discharge to 6 months after discharge

  2. Patient Satisfaction with airway clearance modality

    survey of satisfaction with prescribed airway clearance modality

    Measured: 10 minutes after each discharge during study period

  3. Length of admission

    length of admission in days

    Measured: usually 10-14 days

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted24 Aug 2017
  2. Study startJul 2018 (estimated)
  3. Primary completion31 Aug 2018 (estimated)
  4. Study completion30 Oct 2018 (estimated)

Why it stopped: Not renewed with IRB

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Double blind
Who is masked
Participant, Outcomes assessor
Enrolment
0 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT03261219
Sponsor's protocol ID
IRB201700115
Status last verified
Oct 2018
First submitted
22 Aug 2017
Last updated
19 Oct 2018
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
Yes
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing Intrapulmonary Percussive ventilation and Chest Physiotherapy Vest (Incourage) in people with Cystic Fibrosis and Airway Clearance Impairment, run by University of Florida.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: withdrawn, as of the sponsor's last update on 19 Oct 2018. Status can change between updates, so confirm with the study contact before making plans.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study was withdrawn before enrolling participants, so there are no results.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

FEV1 change (time frame: duration of hospital stay (usually 10-14 days)). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 19 Oct 2018.

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IPV vs CPT for Airway Clearance During CF Exacerbation | AzTrials