AsthmaPhase 4RECONSTRUCTNCT03034005
The RECONSTRUCT Study - Reconstructing Disease Mechanisms in Asthma
A Phase 4 study testing Budesonide in people with Asthma, run by Bispebjerg Hospital at 1 site in Denmark.
Trial summary
This study aims to assess the effect of inhaled corticosteroids (ICS) on airway smooth muscle (ASM) Na+, K+ pumps in patients with asthma.We wish to investigate differences in Na+, K+ pump content in healthy versus asthmatic patients, whether a reduction in airway hyper-responsiveness observed in asthmatic patients… Read more about this study
- Who is it for?
- Ages 18 to 64 yearsHealthy volunteers can take part
- Conditions the study is for
- Asthma
- What is being tested?
- Budesonide
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 60 participants
- Where
- 1 siteDenmark
- Study dates
- 27 Mar 2017to 28 Feb 2019
- Phase
- Phase 4
- 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 to 64 years
- All sexes
- Healthy volunteers accepted
- Adult
Who may be able to join
- Asthma as defined by GINA (www.ginasthma.org) Eosinophilic asthma: Fractional exhaled nitric oxide (FeNO) > 25 ppb (marker of eosinophilic airway inflammation) Non-eosinophilic asthma: Fractional exhaled nitric oxide (FeNO) < 25 ppb
- An FEV1 value of ≥70% of expected
- Airway hyperresponsiveness to mannitol (PD15 ≤ 315 mg)
- Not treated with oral or inhaled steroids (past 3 months)
Who cannot join
- Smoking (current smokers or a maximum of 10 pack years)
- Competing respiratory diseases
- Lower respiratory tract infection within the past 4 weeks
- Medical history with significant comorbidity (ASA>2)
- Pregnant or breastfeeding
- Hypersensitivity to study medication including Spirocort, Osmohale, Midazolam or Fentanyl
Show all 11Show fewer
- Uncontrolled hypertension
- Acute myocardial infarction within past 6 months
- Aorta- or cerebral aneurism
- Recent abdominal operation
- Failure to comply with study protocol
Trial locations and contacts
1 site in 1 country.
Denmark1 site
Lungemedicinsk forskningsenhed, Bispebjerg Hospital
Copenhagen, 2400
About this study
This study aims to assess the effect of inhaled corticosteroids (ICS) on airway smooth muscle (ASM) Na+, K+ pumps in patients with asthma.We wish to investigate differences in Na+, K+ pump content in healthy versus asthmatic patients, whether a reduction in airway hyper-responsiveness observed in asthmatic patients treated with ICS is attributable to an increase in Na+, K+ pump content in ASM cells and compare this in patients with non-eosinophilic asthma versus eosinophilic asthma.
Read the detailed description
Purpose and background
Inhaled corticosteroids and asthma phenotypes Inhaled corticosteroid (ICS) is a cornerstone in the treatment of asthma. ICS acts locally in the airways through several pathways to limit inflammation, primarily through reduction of eosinophilic inflammation.
In clinical practice however a substantial part of adult patients with asthma have no eosinophilic inflammation in the airways despite reduced lung function and increased contractility of the smooth muscles in the airways i.e., airway hyperresponsiveness(AHR). This group of patients with non-eosinophilic asthma (NEA) represents up to 50 % of adult asthmatics with even higher occurrence among patients referred to a specialist.
The effect of ICS in NEA is debated but despite lack of eosinophilic inflammation, ICS has been shown to significantly reduce AHR in patients with NEA, suggesting mechanistic pathways different from reduction in eosinophilic inflammation.
Airway smooth muscle and inhaled corticosteroids Airway smooth muscle (ASM) is the most abundant tissue type in the airways. It plays a crucial part in the pathogenesis of asthma and serves as an important target for therapy especially with β-adrenergic agents and to some extent anti-muscarinic agents, counteracting bronchoconstriction. However also ICS has been proposed to have direct action on ASM cells affecting contractility through reduction of intracellular Ca2+ or down regulation of membrane bound receptors as well as through limiting cellular proliferation and secretory function. The bronchodilating effect of β-adrenergic agents has in animal models shown to be potentiated by administration of corticosteroids.
Inhaled corticosteroids and the Na+, K+ pump Both ICS and systemically administered prednisone has been shown to increase Na+, K+ pump activity in leucocytes from patients with asthma and in both rats and humans systemically administered corticosteroid increases the amount of Na+, K+ pumps in striated muscle by 20-40 % and 30-60 % respectively. We have recently demonstrated a similar effect with ICS where a therapeutically relevant daily dose of 1600 μg budesonide, administered in the respiratory tract by inhalation, increased the amount of Na+, K+ pumps in striated muscle by 17 %.
1.1.4 The Na+, K+ pump and airway smooth muscle The Na+, K+ pump creates an inward Na+ current by removing Na+ from the intracellular lumen of cells. This may drive extrusion of Ca2+ from the lumen of the ASM cells through the Na+, Ca2+ exchanger lowering intracellular Ca2+ concentration. Since Ca2+ plays a central role in smooth muscle contraction, lower intracellular concentrations may protect against bronchoconstriction as well as the contrary might reinforce AHR.
In vitro studies have demonstrated disturbances in leucocyte Na+, K+ pump activity and increased intracellular Na+ in patients with hyperreactivity and asthma. Likewise in vitro studies of human bronchial muscle have shown increased AHR and concentrations of intracellular Ca2+ as well as decreased β-adrenergic induced relaxation of human bronchial muscle when Na+, K+ pumps are blocked.
Bronchoconstriction and airway remodeling are universal features of asthma and especially bronchoconstriction can to some extent be related to proposed disturbances in Na+, K+ pump activity and positive effects of ICS besides being anti-inflammatory is therefore suspected to be beneficial independent of cellular patterns. However the non-inflammatory effect might be more evident in patients with NEA since it is not blurred by the anti-inflammatory effect seen in patients with EA.
No studies have assessed the effect of ICS on ASM Na+, K+ pumps in patients with asthma. In the present study the investigators wish to study differences in Na+, K+ pump content in healthy versus asthmatic patients, whether a reduction in AHR observed in asthmatic patients treated with ICS is attributable to an increase in Na+, K+ pump content in ASM cells and compare this in patients with NEA versus EA.
This results in a study in two parts:
- A comparison of the level of Na+, K+ pumps in ASM in patients with asthma vs healthy subjects.
II. A description of the association between changes in Na+, K+ pump content in ASM and change in AHR after ICS in patients with asthma.
Hypothesis Study part I: The amount of ASM Na+, K+ pumps are lower in adult patients with asthma compared to healthy subjects.
Study part II: The reduction in airway hyperresponsiveness in adult patients with asthma after treatment with ICS is related to an increase in the content of Na+, K+ pumps in ASM.
We further hypothesize that the association between the increase in Na+, K+ pumps in ASM and the change in AHR after ICS treatment is strongest in NEA versus EA.
Aim Study part I: To describe differences in ASM content of Na+, K+ pumps among healthy subjects and patients with NEA or EA respectively.
Study part II: To describe the correlation between increase in ASM content of Na+, K+ pumps and reduction in airway hyperresponsiveness to mannitol after six weeks of daily inhalation of glucocorticoid, in patients with asthma.
Perspectives Asthma is common and may be difficult to treat, especially the non-eosinophilic phenotype. This study aims to increase our understanding of pathogenic mechanisms in asthma, unrelated to inflammatory pathways. This may lead towards a shift from the current paradigm of asthma as a purely inflammatory condition, creating novel understanding of the role of ion transport regulation in the pathogenesis and treatment of asthma, ultimately revealing targets for novel treatments.
- Conditions
- Asthma
- Being tested
- Budesonide
- Keywords
- Inhaled corticosteroids, Airway hyper-responsiveness, Airway smooth muscle, sodium-potassium pump
- Medical subject headings
- Asthma, Respiratory Hypersensitivity
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
BudesonideDrug
Also called Pulmicort
1600 ug inhaled daily for 6 weeks
| Study group | Role | What they receive |
|---|---|---|
| Patients with asthma | Experimental | 6 weeks treatment with 1600 ug budesonide Receives: Drug: Budesonide |
| Healthy Controls | No intervention | Healthy controls to establish baseline level of Na/K pumps. |
What is being measured
The primary outcome is the main question the study is designed to answer.
Change in airway hyperresponsiveness (mannitol challenge) per change in Na+, K+ pumps content in airway smooth muscle.
Change in PD15 per chhange in NA/K ATP'ase content
Measured: 6 weeks
Secondary outcomes (2)
Change in Na+, K+ pump content in airway smooth muscle and in skeletal muscle (ρmol ouabain per g wet weight) in NEA vs. EA.
Change in Na+, K+ pump content in airway smooth muscle and in skeletal muscle (ρmol ouabain per g wet weight) in NEA vs. EA.
Measured: 6 weeks
Change in airway hyperresponsiveness (PD15 to mannitol) in NEA vs. EA
Change in airway hyperresponsiveness (PD15 to mannitol) in NEA vs. EA
Measured: 6 weeks
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted27 Jan 2017 (estimated)
- Study start27 Mar 2017
- Primary completion28 Feb 2019
- Study completion28 Feb 2019
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for AsthmaStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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 4
- Primary purpose
- Treatment
- Allocation
- Non-randomised
- Intervention model
- Single group
- Masking
- None (open label)
- Enrolment
- 60 participants (actual)
Sponsor and investigators
- Lead sponsor
- Bispebjerg Hospital
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Celeste Porsbjerg, Bispebjerg Hospital
- Investigators
- Celeste Porsbjerg, Principal investigator, Assistant Professor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT03034005
- Sponsor's protocol ID
- 2016-003509-33
- Other IDs
- 2016
- Acronym
- RECONSTRUCT
- Status last verified
- Feb 2023
- First submitted
- 25 Jan 2017
- Last updated
- 10 Feb 2023
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 10 Feb 2023. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- The RECONSTRUCT Study - Reconstructing Disease Mechanisms in Asthma
- ClinicalTrials.gov ID
- NCT03034005
- Acronym / sponsor ID
- RECONSTRUCT / 2016-003509-33
- Conditions
- Asthma
- Keywords
- Inhaled corticosteroids, Airway hyper-responsiveness, Airway smooth muscle, sodium-potassium pump
- Phase
- Phase 4
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 60 participants (actual)
- Lead sponsor
- Bispebjerg HospitalUniversity, hospital or other
- Study start
- 27 Mar 2017 (actual)
- Primary completion
- 28 Feb 2019 (actual)
- Study completion
- 28 Feb 2019 (actual)
- First posted
- 27 Jan 2017 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
This study aims to assess the effect of inhaled corticosteroids (ICS) on airway smooth muscle (ASM) Na+, K+ pumps in patients with asthma.We wish to investigate differences in Na+, K+ pump content in healthy versus asthmatic patients, whether a reduction in airway hyper-responsiveness observed in asthmatic patients treated with ICS is attributable to an increase in Na+, K+ pump content in ASM cells and compare this in patients with non-eosinophilic asthma versus eosinophilic asthma.
Detailed description
Purpose and background
Inhaled corticosteroids and asthma phenotypes Inhaled corticosteroid (ICS) is a cornerstone in the treatment of asthma. ICS acts locally in the airways through several pathways to limit inflammation, primarily through reduction of eosinophilic inflammation.
In clinical practice however a substantial part of adult patients with asthma have no eosinophilic inflammation in the airways despite reduced lung function and increased contractility of the smooth muscles in the airways i.e., airway hyperresponsiveness(AHR). This group of patients with non-eosinophilic asthma (NEA) represents up to 50 % of adult asthmatics with even higher occurrence among patients referred to a specialist.
The effect of ICS in NEA is debated but despite lack of eosinophilic inflammation, ICS has been shown to significantly reduce AHR in patients with NEA, suggesting mechanistic pathways different from reduction in eosinophilic inflammation.
Airway smooth muscle and inhaled corticosteroids Airway smooth muscle (ASM) is the most abundant tissue type in the airways. It plays a crucial part in the pathogenesis of asthma and serves as an important target for therapy especially with β-adrenergic agents and to some extent anti-muscarinic agents, counteracting bronchoconstriction. However also ICS has been proposed to have direct action on ASM cells affecting contractility through reduction of intracellular Ca2+ or down regulation of membrane bound receptors as well as through limiting cellular proliferation and secretory function. The bronchodilating effect of β-adrenergic agents has in animal models shown to be potentiated by administration of corticosteroids.
Inhaled corticosteroids and the Na+, K+ pump Both ICS and systemically administered prednisone has been shown to increase Na+, K+ pump activity in leucocytes from patients with asthma and in both rats and humans systemically administered corticosteroid increases the amount of Na+, K+ pumps in striated muscle by 20-40 % and 30-60 % respectively. We have recently demonstrated a similar effect with ICS where a therapeutically relevant daily dose of 1600 μg budesonide, administered in the respiratory tract by inhalation, increased the amount of Na+, K+ pumps in striated muscle by 17 %.
1.1.4 The Na+, K+ pump and airway smooth muscle The Na+, K+ pump creates an inward Na+ current by removing Na+ from the intracellular lumen of cells. This may drive extrusion of Ca2+ from the lumen of the ASM cells through the Na+, Ca2+ exchanger lowering intracellular Ca2+ concentration. Since Ca2+ plays a central role in smooth muscle contraction, lower intracellular concentrations may protect against bronchoconstriction as well as the contrary might reinforce AHR.
In vitro studies have demonstrated disturbances in leucocyte Na+, K+ pump activity and increased intracellular Na+ in patients with hyperreactivity and asthma. Likewise in vitro studies of human bronchial muscle have shown increased AHR and concentrations of intracellular Ca2+ as well as decreased β-adrenergic induced relaxation of human bronchial muscle when Na+, K+ pumps are blocked.
Bronchoconstriction and airway remodeling are universal features of asthma and especially bronchoconstriction can to some extent be related to proposed disturbances in Na+, K+ pump activity and positive effects of ICS besides being anti-inflammatory is therefore suspected to be beneficial independent of cellular patterns. However the non-inflammatory effect might be more evident in patients with NEA since it is not blurred by the anti-inflammatory effect seen in patients with EA.
No studies have assessed the effect of ICS on ASM Na+, K+ pumps in patients with asthma. In the present study the investigators wish to study differences in Na+, K+ pump content in healthy versus asthmatic patients, whether a reduction in AHR observed in asthmatic patients treated with ICS is attributable to an increase in Na+, K+ pump content in ASM cells and compare this in patients with NEA versus EA.
This results in a study in two parts:
- A comparison of the level of Na+, K+ pumps in ASM in patients with asthma vs healthy subjects.
II. A description of the association between changes in Na+, K+ pump content in ASM and change in AHR after ICS in patients with asthma.
Hypothesis Study part I: The amount of ASM Na+, K+ pumps are lower in adult patients with asthma compared to healthy subjects.
Study part II: The reduction in airway hyperresponsiveness in adult patients with asthma after treatment with ICS is related to an increase in the content of Na+, K+ pumps in ASM.
We further hypothesize that the association between the increase in Na+, K+ pumps in ASM and the change in AHR after ICS treatment is strongest in NEA versus EA.
Aim Study part I: To describe differences in ASM content of Na+, K+ pumps among healthy subjects and patients with NEA or EA respectively.
Study part II: To describe the correlation between increase in ASM content of Na+, K+ pumps and reduction in airway hyperresponsiveness to mannitol after six weeks of daily inhalation of glucocorticoid, in patients with asthma.
Perspectives Asthma is common and may be difficult to treat, especially the non-eosinophilic phenotype. This study aims to increase our understanding of pathogenic mechanisms in asthma, unrelated to inflammatory pathways. This may lead towards a shift from the current paradigm of asthma as a purely inflammatory condition, creating novel understanding of the role of ion transport regulation in the pathogenesis and treatment of asthma, ultimately revealing targets for novel treatments.
Study design
- Primary purpose
- Treatment
- Allocation
- Non-randomised
- Intervention model
- Single group
- Masking
- None (open label)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Patients with asthma | Experimental | Drug: Budesonide6 weeks treatment with 1600 ug budesonide |
| Healthy Controls | No intervention | –Healthy controls to establish baseline level of Na/K pumps. |
Who may qualify
- Ages
- 18 to 64 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult
Key inclusion criteria (4 listed)
- Asthma as defined by GINA (www.ginasthma.org) Eosinophilic asthma: Fractional exhaled nitric oxide (FeNO) > 25 ppb (marker of eosinophilic airway inflammation) Non-eosinophilic asthma: Fractional exhaled nitric oxide (FeNO) < 25 ppb
- An FEV1 value of ≥70% of expected
- Airway hyperresponsiveness to mannitol (PD15 ≤ 315 mg)
- Not treated with oral or inhaled steroids (past 3 months)
Key exclusion criteria (11 listed)
- Smoking (current smokers or a maximum of 10 pack years)
- Competing respiratory diseases
- Lower respiratory tract infection within the past 4 weeks
- Medical history with significant comorbidity (ASA>2)
- Pregnant or breastfeeding
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| BudesonideAlso: Pulmicort1600 ug inhaled daily for 6 weeks | Drug | Patients with asthma |
Primary outcome
Change in airway hyperresponsiveness (mannitol challenge) per change in Na+, K+ pumps content in airway smooth muscle.
Time frame: 6 weeks
Change in PD15 per chhange in NA/K ATP'ase content
2 secondary outcomes
Change in Na+, K+ pump content in airway smooth muscle and in skeletal muscle (ρmol ouabain per g wet weight) in NEA vs. EA.
Time frame: 6 weeks
Change in airway hyperresponsiveness (PD15 to mannitol) in NEA vs. EA
Time frame: 6 weeks
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 10 Feb 2023.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Celeste Porsbjerg principal investigator
Assistant Professor
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 4 study testing Budesonide in people with Asthma, run by Bispebjerg Hospital at 1 site in Denmark.
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 4 inclusion and 11 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: finished, as of the sponsor's last update on 10 Feb 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 Denmark. 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.
What does this phase mean?
Phase 4 studies take place after a treatment is approved, to learn more about its long-term benefits and risks in everyday use.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
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?
Change in airway hyperresponsiveness (mannitol challenge) per change in Na+, K+ pumps content in airway smooth muscle. (time frame: 6 weeks). 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 Feb 2023.