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DiaphragmEVELHYNNCT03827538

Endobronchial Valves Positioning Effects On Diaphragm Function In Patients With Lung Hyperinflation

An observational study of Diaphragm, run by University of Modena and Reggio Emilia at 1 site in Italy.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

This prospective study aims at evaluating diaphragmatic function before and after endobronchial valves positioning in a COPD patients with lung hyperinflation. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Diaphragm
How many people
30 participants
Where
1 siteItaly
Study dates
1 Oct 2019to 31 Dec 2024
Phase
Observational
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 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: See inclusion criteria

Who may be able to join

  • age> 18
  • patient admission for intervention for endobronchial valves positioning due to documented lung hyperinflation.

Who cannot join

  • previously documented diaphragmatic dysfunction
  • the presence of neuromuscular diseases or other forms of myopathy
  • pregnancy
  • lack of collaboration in performing functional diaphragmatic tests

Trial locations and contacts

1 site in 1 country.

Italy1 site, 1 recruiting
  • University Hospital of Modena Policlinico

    Modena, 41125

    Alessandro Marchioni, MD, PhD, marchioni.alessandro@unimore.it

    Recruiting

Other trials in Italy

About this study

Official title: Endobronchial Valves Positioning Effects On Diaphragm Function In Patients With Lung Hyperinflation - EVELHYN

This prospective study aims at evaluating diaphragmatic function before and after endobronchial valves positioning in a COPD patients with lung hyperinflation.

Read the detailed description

Data obtained from clinical and bimolecular studies have showed that chronic obstructive pulmonary disease (COPD) patients might present higher rates of diaphragm function impairment when compared to age and sex matched healthy controls. The potential mechanisms of injury have been found in regional stresses and strains due to disadvantageous muscle geometry, increased workload during exertion, mechanical stress and metabolic factors (i.e., increased protease activity, free radicals, oxidation). In particular emphysema, with the breakdown of elastic alveolar tissue, leads to increased lung compliance and gas trapping. Lung hyperinflation with amplified dynamic elastance and intrinsic positive end expiratory pressure (PEEPi) limit the diaphragmatic excursion capacity. Moreover both end expiratory lung volume (EELV) and residual volume (RV) increase, shifting tidal breathing (Vt) towards the right side of the pressure-volume curve and imposing higher intra-thoracic pressures to maintain an adequate Vt. Furthermore it has been showed that in COPD patients experiencing frequent exacerbations the maximum pressure produced by diaphragm contraction seems significantly lower as compared to non-COPD subjects, independently on the nature of the tests used for assessment (both volitional - Pdi at Total Lung Capacity (TLC) or Pdi sniff- or non volitional - phrenic nerve stimulation). Thus the reduction of diaphragm maximal performances might be explained by muscle shortening and mechanical impairment following the onset of progressive lung hyperinflation. Lung hyperinflation worsens with exercise leading to breathlessness and is associated with reduced physical activity and reduced survival. Inhaled bronchodilator medications have only modest impacts on symptoms and do not alter the natural history of the disease. In selected patients with a heterogeneous pattern of emphysema, surgical resection can be targeted at the worst affected areas of lung tissue, which contribute disproportionately to gas trapping and hyperinflation, and so improve respiratory mechanics. Lung volume reduction surgery in selected patients (LVRS) improves symptoms and prolongs survival but can be associated with significant morbidity and a risk of death, with a cost per quality adjusted life year (QALY) of at least $40 000.

A more recent approach has been to use endobronchial valves to occlude the airways supplying the worst affected part of the lung. This is intended to cause atelectasis in the target lobe, with a similar impact on the function of the rest of the lung as seen in LVRS. Several trials have demonstrated that endobronchial valve treatment in patients with emphysema can lead to improvements in symptoms, lung function and exercise capacity reductions in dynamic hyperinflation and improvements in oxygen kinetics and chest wall synchrony. While studies on surgical lung volume reduction have demonstrated improvement in diaphragmatic muscle function no studies have investigated the effects of endobronchial valves positioning on diaphragm performance in patients with lung hyperinflation.

Several methods have been used to evaluate diaphragmatic contractile activity. Among these, the standard reference is represented by the measurement of trans-diaphragmatic (Pdi) pressure expressed by the difference between pleural (or esophageal [Pes]) and abdominal (or gastric [Pgas]) pressures through nasogastric probes equipped with pressure sensors. However, such methods are still far from routine clinical practice, thus highlighting the need for simple and accurate methods to assess diaphragmatic performance. In last years the ultrasound (US) evaluation of the diaphragmatic function has been developing in the field of intensive care as a tool to estimate patient's work of breathing during ventilation. In a recently published study on 75 patients with AECOPD requiring mechanical ventilation, we showed a complete correlation between US assessment and Pdi measurements at maximal inspiration in evaluating diaphragm function. In particular we demonstrated that changes of the diaphragm thickness (ΔTdi) < 20% during tidal volume has the same accuracy of transdiaphragmatic pressure in identifying diaphragm impairment. Furthermore we investigated the US evaluation of the diaphragm in patients with amyotrophic lateral sclerosis (ALS) through the ΔTmax index (the ratio between diaphragm thickness at the end of Vt and after maximal inspiration up to total lung capacity). We found that ΔTmax strongly correlates with respiratory functions tests with high accuracy in identifying subjects with FVC <50% of predicted value. Moreover in a recently published study, Bernardi and coworkers presented a non invasive technique to measure PEEPi in COPD patients, through the US assessment of the time latency (msec) between the onset of diaphragm contraction on US and the onset of inspiratory flow (28).

This prospective study aims at evaluating diaphragmatic function before and after endobronchial valves positioning in a COPD patients with lung hyperinflation.

Materials and methods Study population and setting This prospective explorative observational cohort study will be carried out in the Thoracic Endoscopic Unit (TEU) of the University Hospital of Modena Italy over a 24-month period once approval from the local Ethics Committee of Modena will be obtained. Written informed consent to participate to the study will be obtained by all enrolled patients patient.

Patients will be eligible if admitted to the TEU for intervention of endobronchial valves positioning due to documented lung hyperinflation.

Exclusion criteria will include previously documented diaphragmatic dysfunction, the presence of neuromuscular diseases or other forms of myopathy.

All patients will be treated according to the best current clinical practice by the TEU staff, which will be blinded to the purpose of the study.

General measures At enrollment respiratory clinical variables (age, sex, diagnosis and stage, body mass index, smoke habits, comorbidities, previous treatment with systemic steroids) and respiratory function test values will be recorded.

Study procedures A respiratory physician with high expertise in chest US will perform a US assessment of the diaphragm before and after endobronchial valves placement. Motility of the diaphragm is assessed with a B-mode US device (GE Vivid 7, Yorba Linda, CA, USA) connected to a 7-12 MHz linear probe. Measurements are performed in supine position with an average inclination of 45°. The position of the probe is set to obtain the best view of the zone of apposition of the diaphragm, located between the mid-axillary and the posterior axillary line. The diaphragm is identified as a three-layer structure consisting of one relatively non-echogenic muscle layer coated in two echogenic lines determined by peritoneal serosa and diaphragmatic pleura. Diaphragm thickness is measured bilaterally at end-inspiration and end-expiration. The US images will be stored in electronic or paper format by an examiner unaware of the purpose of the study.

In particular the following measurements will be performed:

  • ΔTd: change in diaphragm thickness (Tdi) during inspiration starting from FRC to Vt = [(end-inspiratory Tdi - end-expiratory Tdi) / end-expiratory Tdi] X 100)
  • ΔTmax: ratio between Tdi at the end of Vt and Tdi after maximal inspiration up to TLC = end-inspiratory Vt Tdi / end-inspiratory TLC Tdi.
  • PEEPiecho: P0.1Mx(TLAT,US/100). TLAT = time latency (msec) between the onset of diaphragm contraction on ultrasound and the onset of inspiratory flow; P0.1M = mouth occlusion pressure at 100ms, an estimate of the effort a patient must make to generate the inspiratory flow. It is measured using a unidirectional valve, occluded during expiration so that the P0.1M is measured from functional residual capacity (FRC).
  • US measurement of maximal diaphragmatic inspiratory excursion measured in right subcostal window.

An assessment of maximal expiratory pressure (MEP) and maximal inspiratory pressure (MIP), and sniff inspiratory nasal pressure (SNIP), will be performed before and after endobronchial valves placement by a respiratory function technician unaware of the purpose of the study.

Each outcome measurements will be performed 24 hours, 48 hours, 7 days, 30 days, 60 days and 90 days after endobronchial valves placement.

Statistical analysis The statistical package GraphPad Prism 7.0 (GraphPad Software, Inc. La Jolla, CA, USA) will be used for analysis. Descriptive statistics for continuous variables will be presented as mean values ± standard deviation (SD) or associated to interquartile range. The nonparametric Wilcoxon test (Mann-Whitney) and t student test will be used for comparison of continuous variables.

Conditions
Diaphragm

What is being measured

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

  1. Diaphrgam function test modification after ELVR

    Ultrasound assessed ΔTdi values change after ELVR

    Measured: 90 days

  2. Diaphrgam fatigue test modification after ELVR

    Ultrasound assessed ΔTmax values change after ELVR

    Measured: 90 days

  3. Diaphrgam performance test modification after ELVR

    Ultrasound assessed PEEPiecho values change after ELVR

    Measured: 90 days

  4. Diaphrgam motion test modification after ELVR

    US assessed maximal diaphragmatic inspiratory excursion after ELVR

    Measured: 90 days

Timeline

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

  1. First posted1 Feb 2019
  2. Study start1 Oct 2019
  3. Primary completion31 Dec 2023 (estimated)
  4. Study completion31 Dec 2024 (estimated)

Resources

More details

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

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
30 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT03827538
Sponsor's protocol ID
UModenaReggio 2
Acronym
EVELHYN
Status last verified
May 2023
First submitted
28 Jan 2019
Last updated
10 May 2023
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided

Questions about this trial

What is this clinical trial studying?

An observational study of Diaphragm, run by University of Modena and Reggio Emilia at 1 site in Italy.

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 2 inclusion and 4 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: status not confirmed, as of the sponsor's last update on 10 May 2023. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Italy. Whether a site is taking part right now should be confirmed with that site. See every site.

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?

Results are not available in the source record.

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

Contact Marchioni Alessandro (00390594225859, marchioni.alessandro@unimore.it), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Diaphrgam function test modification after ELVR (time frame: 90 days). The study lists 4 primary outcomes in all. 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 10 May 2023.

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