Chronic Obstructive Pulmonary DiseaseRECONSIDERNCT02652559
Initiation of Long-term Non-invasive Ventilation in COPD
A study testing Transcutaneous measurements of PCO2, Telemonitoring and EMG in people with Chronic Obstructive Pulmonary Disease, run by University Medical Center Groningen at 1 site in Netherlands.
Trial summary
Rationale: Application of long-term non-invasive ventilation (NIV) in stable chronic obstructive pulmonary disease (COPD) patients with chronic hypercapnic respiratory failure (CHRF) has recently been shown to improve survival and quality of life when applied with sufficiently high inspiratory pressures and adequate… Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Chronic Obstructive Pulmonary Disease
- What is being tested?
- Transcutaneous measurements of PCO2, Telemonitoring and EMG
- Type of treatment
- Medical device
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 67 participants
- Where
- 1 siteNetherlands
- Study dates
- Jun 2016to 25 Jul 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 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Indication to initiate chronic NIV in COPD patients (GOLD stage III or IV: FEV1/ forced vital capacity (FVC)< 70% and FEV1< 50% predicted; PaCO2 > 6.0 kPa in stable condition, which means no COPD exacerbation for 4 weeks and a pH > 7.35)
- Age > 18 years
- Existence of a sufficient social support network making initiation of HMV at home possible and safe.
Who cannot join
- Instable severe cardiac comorbidities (left ventricular ejection fraction below 45%, instable angina pectoris complaints)
- Patients admitted to a nursing home
Trial locations and contacts
1 site in 1 country.
About this study
Official title: Treatment of Chronic Respiratory Failure in COPD Patients With Non-invasive Ventilation: Starting at Home and Selecting the Right Patient
Rationale:
Application of long-term non-invasive ventilation (NIV) in stable chronic obstructive pulmonary disease (COPD) patients with chronic hypercapnic respiratory failure (CHRF) has recently been shown to improve survival and quality of life when applied with sufficiently high inspiratory pressures and adequate backup breathing frequencies (so called high-intensity NIV). However, for a broader implementation of this therapy in a potentially large group of patients, important issues have to be solved. First, the initiation of high-intensity NIV, currently performed in the hospital, is often time-consuming, expensive and inconvenient for patients. Secondly, although clinicians recognise that not all patients benefit, it is not known which factors predict a positive response.
Read more
Objectives:
- To investigate whether home initiation of chronic NIV in stable COPD patients with CHRF is non-inferior to inpatient initiation.
- To investigate predictors of a favourable response to chronic NIV in COPD patients with CHRF.
Study design:
The study is 1:1 two-arm parallel group randomised controlled trial comparing the usual inpatient NIV initiation to home initiation.
Study population: Seventy-two COPD patients with a NIV indication (COPD GOLD stage III or IV; partial arterial carbon dioxide pressure (PaCO2) > 6.0 kPa in stable condition, i.e. no COPD exacerbation for 4 weeks and a pH > 7.35), a sufficient social network at home, without severe cardiac comorbidities, will be included.
Intervention: Home initiation of NIV will be compared with standard in-hospital initiation. NIV at home will be titrated by a specialised nurse of our home mechanical ventilation centre (HMV) on transcutaneously measured gas exchange and respiratory electromyography and will be adjusted with the use of telemedicine.
Main study parameters/endpoints:
- To investigate non-inferiority of home initiation, the change in arterial carbon dioxide pressure after 3 months treatment will be the primary outcome. Secondary outcomes are safety, change in lung function, health-related quality of life (HRQoL) and costs.
- To investigate predictors of a favourable response, patient demographics, and baseline data on lung function as well as measures of respiratory muscle activity, arterial blood gases, comorbidities, inflammatory blood markers and anxiety and depressions scores will be collected of all patients.
Read the detailed description
COPD is a chronic disease with high mortality and morbidity worldwide. Patients with end-stage COPD frequently develop CHRF associated with end-of-life. In that stage of disease, treatment options are limited.
Long-term nocturnal NIV has been applied in patients with chronic alveolar hypoventilation for decades. While there is no doubt that applying chronic nocturnal NIV improves outcomes in patients with restrictive and neuromuscular diseases, the evidence in COPD patients has long been controversial. At the HMV centre Groningen, the majority of patients treated with NIV therefore still concerns patients with neuromuscular diseases.
Initial trials investigating chronic NIV in COPD showed no relevant benefits, neither in terms of improvement in gas exchange nor in improvements in patient-centred outcomes as HRQoL.However, most of these trials used low inspiratory pressures so that improvement of alveolar hypoventilation was not or only partially achieved. Consequently, little improvement in clinical outcomes could be expected.
More than 10 years ago, the concept of high-intensity NIV in COPD was introduced. By applying higher inspiratory pressures and breathing frequencies aimed at a more controlled form of ventilation and improvement in gas exchange, clinically relevant improvements in HRQoL and lung function were observed, without undue loss of patient comfort. Recently, a German group conclusively showed that high-intensity NIV improves survival in severe COPD patients with CHRF. These positive results with high-intensity NIV have changed our view towards the use of chronic NIV in stable COPD. Nowadays, the investigators believe that the evidence for long-term nocturnal NIV is convincing and justifies the application of this therapy in patients with severe stable COPD patients with CHRF. Nevertheless, for a broader implementation of this treatment in a potentially large group of severe COPD patients, important issues have to be solved.
First, the current inpatient NIV initiation process has to be reconsidered, which despite tight titration based on arterial blood gases, does not always lead to good patient compliance, is inconvenient for patients and is expensive. While it might be thought that high-intensity NIV necessitates inpatient titration to gain adequate reversal of hypoventilation, different in hospital set ups of NIV initiation (on a general ward, medium care unit or on an intensive care unit), with different ways of titration (guided by transcutaneous carbon dioxide (PtCO2) or arterial blood gases (PaCO2)), have not resulted in different outcomes or a different compliance at the long-term. Also, these inpatient options are expensive as initiation of NIV in COPD routinely requires 5-14 days. Recently, our group of the HMV centre Groningen has shown that, in patients with neuromuscular and restrictive thoracic diseases, initiation of NIV can safely be performed at home. Initiation of NIV at home was preferred by the patients, was equally effective and saved costs compared to inpatient initiation. Importantly, COPD patients have been excluded in this randomised controlled trial (RCT), as at the start of that study chronic NIV in COPD was not considered a regular standard treatment option in the Netherlands. Furthermore, initiation of NIV in COPD patients at that time was thought to be probably too difficult to be performed at home, because high-intensity NIV is needed in this patient group to improve outcomes.
However, challenges with the initiation of high-intensity NIV require attention, but do not necessarily have to be solved in-hospital. On the one hand, patients with COPD need higher inspiratory pressures and higher backup breathing frequencies as it is more difficult to correct alveolar hypoventilation in lung parenchyma diseases compared to diseases in which the lungs are not primarily affected, such as in neuromuscular disease. On the other hand, the investigators believe that careful high-intensity NIV initiation and titration should not only focus on maximal improvement in PaCO2 but also on patient comfort. The consequence of high-intensity might be that COPD patients need even more time and attention from caregivers to get used to the high pressures and high backup frequencies before our target can be reached, i.e. improvement in gas exchange and respiratory muscle unloading, before the conditions also for a good long-term compliance can be satisfied.
Finding the individual high-intensity setting leading to sufficient improvement in objective physiological parameters is challenging in this group of patients. This process therefore probably requires more frequent and more intensive monitoring. At home, the investigators will optimise monitoring of the patients with the use of frequent non-invasive monitoring of gas exchange with transcutaneous measurements (SenTec DM®, Software V-STATS 4.0; SenTec AG; Therwil, Switzerland). Secondly, analysis of data read from the ventilator software (Respironics Trilogy 202®, Philips, the Netherlands) will be used to provide information about compliance and the actual provided ventilation. Finally, the investigators will aid measurements of respiratory muscle activity by means of surface electromyography (EMG) as a relatively new tool which can aid in optimising NIV initiation. Surface EMG is a new tool that might help to optimise NIV initiation. It has been shown that especially high-intensity NIV is able to unload the respiratory muscles (Duiverman, work in progress).This might importantly add to the achievement of clinical relevant benefits. Until now, no studies have used non-invasive measurements of respiratory muscle unloading to optimise initiation of NIV. In the last decade, I have developed and validated a surface EMG technique for use in COPD patients, measuring respiratory muscle activity as a surrogate of respiratory neural drive and thus muscle loading. As this method is non-invasive, it can easily be applied at home. Furthermore, surface EMG can be used to asses patient-ventilator asynchrony (PVA). Especially with higher inspiratory pressures and/or high breathing frequencies PVA may arise.PVA is important as it leads to increased work of breathing, decreased patient comfort and less effective ventilation. During the traditional in-hospital NIV initiation, one might suggest that an indication of respiratory muscle (un)loading and patient-ventilator synchrony is received through observation of the patient. However, observation by the respiratory nurses is mostly of limited time and detects only events leading to a huge excess of respiratory muscle loading, such as during severe PVA. During home initiation, direct observation is far less easy and less frequent. In concordance with a recent study showing that parasternal EMG can be used to assess PVA in a mixed group of patients initiated on home NIV, the investigators have shown in a recent pilot project that also our surface EMG is feasible to measure respiratory muscle unloading and detect PVA, of note, during different settings, also high-intensity NIV (submitted work). As the use of surface EMG for optimising NIV initiation is relatively new, the investigators will extend the monitoring of patients in both groups including surface EMG as a surrogate marker of respiratory muscle unloading and to detect PVA during NIV.
For the second issue, the necessity for acclimatisation time and caregiver attention, very elegant solutions are available to provide this at home too. A longer initiation period can better be met at home, in a trusted environment for the patient, saving the disadvantages and costs of a prolonged hospital stay. With modern technologies the necessary caregiver attention can also be provided at home. Monitoring data can be sent to caregivers on daily basis by telemonitoring. This proven technology enables caregivers to make on daily basis, on distance, decisions regarding the NIV initiation process, which will be discussed with the patient by frequent telephone calls. This so called telemedicine has already been shown to be a valuable and promising tool to monitor and to adjust treatment of patients already established on chronic NIV at home. In our home NIV initiation pilot project in neuromuscular patients, the investigators were the first to show in a RCT that this technology was very feasible to use for NIV initiation at home.
The second important issue to be solved regards better patient selection. By collecting the baseline and follow-up data of the COPD patients initiated on NIV, the investigators aim to find predictors of a favourable response to NIV. It is known, from clinical practice and from studies, that not all patients respond favourably. Until now, data have shown that patients with CHRF benefit. Furthermore, benefits at least in terms of improvement in gas exchange, seem to be more prominent in patients with severe stable hypercapnia. In contrast, our group has shown that patients that remain hypercapnic after an exacerbation do not uniformly benefit. An individual COPD phenotype benefiting most from this demanding therapy has not been identified.
The aim of the present study is to investigate whether home initiation of chronic NIV in stable COPD patients with CHRF is non-inferior to inpatient initiation in terms of improvement in PaCO2 after 6 months.
Secondary outcomes are change in lung function (forced expiratory volume in 1 second (FEV1), lung volumes (total lung capacity (TLC), residual volume (RV) and RV%TLC), and diffusion capacity (DLCO (%predicted)), change in HRQoL, and costs including cost-effectiveness analyses.
The secondary objective of the study is to collect patient demographics (age, weight, height, social status, HRQoL, anxiety and depression scores, data on comorbidities and medication use), respiratory function (lung function as well as measures of respiratory muscle activity, arterial blood gases), and inflammatory blood markers, in order to analyse how differences in baseline parameters are related to changes in HRQoL.
- Conditions
- Chronic Obstructive Pulmonary Disease
- Being tested
- Transcutaneous measurements of PCO2, Telemonitoring, EMG, Home initiation of NIV, Inhospital initiation of NIV
- Keywords
- Chronic Obstructive Pulmonary Disease, Non-invasive ventilation, Home initiation
- Medical subject headings
- Pulmonary Disease, Chronic Obstructive
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Transcutaneous measurements of PCO2Device
PCO2 will be measured transcutaneously with an ear lobe sensor before initiation of NIV, and during the initiation period (SenTec DM®, Software V-STATS 4.0; SenTec AG; Therwil, Switzerland)
TelemonitoringDevice
Telemonitoring will be used to send data from the transcutaneous measurements, data from the EMG measurements and data from the ventilator from home to the hospital.
EMGDevice
Surface EMG of the respiratory muscles will be used to monit patients in both groups as a surrogate marker of respiratory muscle unloading and to detect PVA during NIV
Home initiation of NIVOther
The primary aim of the study is to compare home and inhospital initiation of NIV
Inhospital initiation of NIVOther
The primary aim of the study is to compare home and inhospital initiation of NIV
| Study group | Role | What they receive |
|---|---|---|
| Home initiation | Experimental | Home initiation of long-term NIV will be compared with standard in-hospital initiation. NIV at home will be titrated by a specialised nurse of our home mechanical ventilation centre (HMV) on transcutaneously measured gas exchange and respiratory electromyography and will be adjusted with the use of telemedicine. Receives: Device: Transcutaneous measurements of PCO2; Device: Telemonitoring; Device: EMG; Other: Home initiation of NIV |
| Inhospital initiation | Active comparator | Inhospital initiation of NIV is standard care and in the study will be set as the control arm. Receives: Device: Transcutaneous measurements of PCO2; Device: EMG; Other: Inhospital initiation of NIV |
What is being measured
The primary outcome is the main question the study is designed to answer.
Change in daytime PaCO2
An arterial function will be performed during spontaneous breathing without oxygen after 6 months.
Measured: Baseline, 6 months
Secondary outcomes (9)
Change in FEV1
Change in FEV1, assessed by spirometry, according to the ERS guidelines.
Measured: Baseline, 6 months
Change in health-related quality of life (HRQoL)
HRQoL will be assessed by the Severe Respiratory Insufficiency (SRI) questionnaire. The SRI is a well-known and validated HRQoL questionnaire especially designed for patients with CHRF on HMV.
Measured: Baseline, 6 months
Incremental cost-utility ratio
In the economic evaluation, the primary aim will be to estimate the direct medical costs of the initiation at home compared to the current national guideline of initiating ventilatory support in the hospital. Cost-effectiveness will be investigated by estimating the healthcare costs of home initiation and usual care and the HRQoL gains of the two options. For the purpose of estimating HRQoL gains both the SRI and the EuroQol (EQ-5D) will be assessed, at baseline and after six months follow up. The incremental cost-utility ratio (ICUR) will be calculated
Measured: Baseline, 6 months
Number of participants with treatment-related adverse events
Treatment related adverse events are aerophagia, mask-related problems (skin irritation) or excessive mask leaks.
Measured: Baseline, 3 months and 6 months
Compliance
Compliance with the home ventilator will be read from ventilator counter readings. The mean number of hours use per day is registered.
Measured: Baseline, 3 months and 6 months
Change in exercise tolerance
Exercise tolerance will be assessed with the 6-minute walking test, performed according to the European Respiratory Society/American Thoracic Society guidelines, along a 30 m indoor course, with standardised encouragements given by the investigator. Oxygen will be prescribed in the regular amount advised to the patient during exercise. Oxygen saturation, heart rate, and Borg dyspnoea scores will be assessed prior to the test and at the end of the test for safety reasons. The outcome will be the number of meters walked.
Measured: Baseline, 6 months
Change in hyperinflation
Hyperinflation will be assessed by measuring total lung capacity (TLC) and residual volume (RV), and assessing the RV%TLC ratio, according to the ERS guidelines
Measured: Baseline, 6 months
Change in diffusion capacity
Diffusion capacity will be assessed by measuring carbon monoxide transfer factor, according to the ERS guidelines
Measured: Baseline, 6 months
Change in PaCO2
An arterial function will be performed during spontaneous breathing without oxygen after 3 months.
Measured: Baseline, 3 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted12 Jan 2016 (estimated)
- Study startJun 2016
- Primary completion25 Jul 2018
- Study completion25 Jul 2018
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for Chronic Obstructive Pulmonary DiseaseStudies of the same condition, open and under way.
- More trials run by University Medical Center GroningenThe sponsor's other registered studies.
- 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 N/A
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Enrolment
- 67 participants (actual)
Sponsor and investigators
- Lead sponsor
- University Medical Center Groningen
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Marieke Duiverman, University Medical Center Groningen
- Investigators
- Marieke Duiverman, MD PhD, Principal investigator, University Medical Center Groningen
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT02652559
- Sponsor's protocol ID
- 201600008
- Acronym
- RECONSIDER
- Status last verified
- Dec 2018
- First submitted
- 6 Jan 2016
- Last updated
- 17 Dec 2018
- Results posted
- No
- Data monitoring committee
- Yes
- Individual data sharing
- No
Publications
Duiverman ML, Vonk JM, Bladder G, van Melle JP, Nieuwenhuis J, Hazenberg A, Kerstjens HAM, van Boven JFM, Wijkstra PJ. Home initiation of chronic non-invasive ventilation in COPD patients with chronic hypercapnic respiratory failure: a randomised controlled trial. Thorax. 2020 Mar;75(3):244-252. doi: 10.1136/thoraxjnl-2019-213303. Epub 2019 Sep 4.
PubMed 31484786
Study at a glance
From the registry record, last updated by the sponsor on 17 Dec 2018. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Treatment of Chronic Respiratory Failure in COPD Patients With Non-invasive Ventilation: Starting at Home and Selecting the Right Patient
- ClinicalTrials.gov ID
- NCT02652559
- Acronym / sponsor ID
- RECONSIDER / 201600008
- Conditions
- Chronic Obstructive Pulmonary Disease
- Keywords
- Chronic Obstructive Pulmonary Disease, Non-invasive ventilation, Home initiation
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 67 participants (actual)
- Lead sponsor
- University Medical Center GroningenUniversity, hospital or other
- Study start
- Jun 2016 (actual)
- Primary completion
- 25 Jul 2018 (actual)
- Study completion
- 25 Jul 2018 (actual)
- First posted
- 12 Jan 2016 (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.
Rationale:
Application of long-term non-invasive ventilation (NIV) in stable chronic obstructive pulmonary disease (COPD) patients with chronic hypercapnic respiratory failure (CHRF) has recently been shown to improve survival and quality of life when applied with sufficiently high inspiratory pressures and adequate backup breathing frequencies (so called high-intensity NIV). However, for a broader implementation of this therapy in a potentially large group of patients, important issues have to be solved. First, the initiation of high-intensity NIV, currently performed in the hospital, is often time-consuming, expensive and inconvenient for patients. Secondly, although clinicians recognise that not all patients benefit, it is not known which factors predict a positive response.
Objectives:
- To investigate whether home initiation of chronic NIV in stable COPD patients with CHRF is non-inferior to inpatient initiation.
- To investigate predictors of a favourable response to chronic NIV in COPD patients with CHRF.
Study design:
The study is 1:1 two-arm parallel group randomised controlled trial comparing the usual inpatient NIV initiation to home initiation.
Study population: Seventy-two COPD patients with a NIV indication (COPD GOLD stage III or IV; partial arterial carbon dioxide pressure (PaCO2) > 6.0 kPa in stable condition, i.e. no COPD exacerbation for 4 weeks and a pH > 7.35), a sufficient social network at home, without severe cardiac comorbidities, will be included.
Intervention: Home initiation of NIV will be compared with standard in-hospital initiation. NIV at home will be titrated by a specialised nurse of our home mechanical ventilation centre (HMV) on transcutaneously measured gas exchange and respiratory electromyography and will be adjusted with the use of telemedicine.
Main study parameters/endpoints:
- To investigate non-inferiority of home initiation, the change in arterial carbon dioxide pressure after 3 months treatment will be the primary outcome. Secondary outcomes are safety, change in lung function, health-related quality of life (HRQoL) and costs.
- To investigate predictors of a favourable response, patient demographics, and baseline data on lung function as well as measures of respiratory muscle activity, arterial blood gases, comorbidities, inflammatory blood markers and anxiety and depressions scores will be collected of all patients.
Detailed description
COPD is a chronic disease with high mortality and morbidity worldwide. Patients with end-stage COPD frequently develop CHRF associated with end-of-life. In that stage of disease, treatment options are limited.
Long-term nocturnal NIV has been applied in patients with chronic alveolar hypoventilation for decades. While there is no doubt that applying chronic nocturnal NIV improves outcomes in patients with restrictive and neuromuscular diseases, the evidence in COPD patients has long been controversial. At the HMV centre Groningen, the majority of patients treated with NIV therefore still concerns patients with neuromuscular diseases.
Initial trials investigating chronic NIV in COPD showed no relevant benefits, neither in terms of improvement in gas exchange nor in improvements in patient-centred outcomes as HRQoL.However, most of these trials used low inspiratory pressures so that improvement of alveolar hypoventilation was not or only partially achieved. Consequently, little improvement in clinical outcomes could be expected.
More than 10 years ago, the concept of high-intensity NIV in COPD was introduced. By applying higher inspiratory pressures and breathing frequencies aimed at a more controlled form of ventilation and improvement in gas exchange, clinically relevant improvements in HRQoL and lung function were observed, without undue loss of patient comfort. Recently, a German group conclusively showed that high-intensity NIV improves survival in severe COPD patients with CHRF. These positive results with high-intensity NIV have changed our view towards the use of chronic NIV in stable COPD. Nowadays, the investigators believe that the evidence for long-term nocturnal NIV is convincing and justifies the application of this therapy in patients with severe stable COPD patients with CHRF. Nevertheless, for a broader implementation of this treatment in a potentially large group of severe COPD patients, important issues have to be solved.
First, the current inpatient NIV initiation process has to be reconsidered, which despite tight titration based on arterial blood gases, does not always lead to good patient compliance, is inconvenient for patients and is expensive. While it might be thought that high-intensity NIV necessitates inpatient titration to gain adequate reversal of hypoventilation, different in hospital set ups of NIV initiation (on a general ward, medium care unit or on an intensive care unit), with different ways of titration (guided by transcutaneous carbon dioxide (PtCO2) or arterial blood gases (PaCO2)), have not resulted in different outcomes or a different compliance at the long-term. Also, these inpatient options are expensive as initiation of NIV in COPD routinely requires 5-14 days. Recently, our group of the HMV centre Groningen has shown that, in patients with neuromuscular and restrictive thoracic diseases, initiation of NIV can safely be performed at home. Initiation of NIV at home was preferred by the patients, was equally effective and saved costs compared to inpatient initiation. Importantly, COPD patients have been excluded in this randomised controlled trial (RCT), as at the start of that study chronic NIV in COPD was not considered a regular standard treatment option in the Netherlands. Furthermore, initiation of NIV in COPD patients at that time was thought to be probably too difficult to be performed at home, because high-intensity NIV is needed in this patient group to improve outcomes.
However, challenges with the initiation of high-intensity NIV require attention, but do not necessarily have to be solved in-hospital. On the one hand, patients with COPD need higher inspiratory pressures and higher backup breathing frequencies as it is more difficult to correct alveolar hypoventilation in lung parenchyma diseases compared to diseases in which the lungs are not primarily affected, such as in neuromuscular disease. On the other hand, the investigators believe that careful high-intensity NIV initiation and titration should not only focus on maximal improvement in PaCO2 but also on patient comfort. The consequence of high-intensity might be that COPD patients need even more time and attention from caregivers to get used to the high pressures and high backup frequencies before our target can be reached, i.e. improvement in gas exchange and respiratory muscle unloading, before the conditions also for a good long-term compliance can be satisfied.
Finding the individual high-intensity setting leading to sufficient improvement in objective physiological parameters is challenging in this group of patients. This process therefore probably requires more frequent and more intensive monitoring. At home, the investigators will optimise monitoring of the patients with the use of frequent non-invasive monitoring of gas exchange with transcutaneous measurements (SenTec DM®, Software V-STATS 4.0; SenTec AG; Therwil, Switzerland). Secondly, analysis of data read from the ventilator software (Respironics Trilogy 202®, Philips, the Netherlands) will be used to provide information about compliance and the actual provided ventilation. Finally, the investigators will aid measurements of respiratory muscle activity by means of surface electromyography (EMG) as a relatively new tool which can aid in optimising NIV initiation. Surface EMG is a new tool that might help to optimise NIV initiation. It has been shown that especially high-intensity NIV is able to unload the respiratory muscles (Duiverman, work in progress).This might importantly add to the achievement of clinical relevant benefits. Until now, no studies have used non-invasive measurements of respiratory muscle unloading to optimise initiation of NIV. In the last decade, I have developed and validated a surface EMG technique for use in COPD patients, measuring respiratory muscle activity as a surrogate of respiratory neural drive and thus muscle loading. As this method is non-invasive, it can easily be applied at home. Furthermore, surface EMG can be used to asses patient-ventilator asynchrony (PVA). Especially with higher inspiratory pressures and/or high breathing frequencies PVA may arise.PVA is important as it leads to increased work of breathing, decreased patient comfort and less effective ventilation. During the traditional in-hospital NIV initiation, one might suggest that an indication of respiratory muscle (un)loading and patient-ventilator synchrony is received through observation of the patient. However, observation by the respiratory nurses is mostly of limited time and detects only events leading to a huge excess of respiratory muscle loading, such as during severe PVA. During home initiation, direct observation is far less easy and less frequent. In concordance with a recent study showing that parasternal EMG can be used to assess PVA in a mixed group of patients initiated on home NIV, the investigators have shown in a recent pilot project that also our surface EMG is feasible to measure respiratory muscle unloading and detect PVA, of note, during different settings, also high-intensity NIV (submitted work). As the use of surface EMG for optimising NIV initiation is relatively new, the investigators will extend the monitoring of patients in both groups including surface EMG as a surrogate marker of respiratory muscle unloading and to detect PVA during NIV.
For the second issue, the necessity for acclimatisation time and caregiver attention, very elegant solutions are available to provide this at home too. A longer initiation period can better be met at home, in a trusted environment for the patient, saving the disadvantages and costs of a prolonged hospital stay. With modern technologies the necessary caregiver attention can also be provided at home. Monitoring data can be sent to caregivers on daily basis by telemonitoring. This proven technology enables caregivers to make on daily basis, on distance, decisions regarding the NIV initiation process, which will be discussed with the patient by frequent telephone calls. This so called telemedicine has already been shown to be a valuable and promising tool to monitor and to adjust treatment of patients already established on chronic NIV at home. In our home NIV initiation pilot project in neuromuscular patients, the investigators were the first to show in a RCT that this technology was very feasible to use for NIV initiation at home.
The second important issue to be solved regards better patient selection. By collecting the baseline and follow-up data of the COPD patients initiated on NIV, the investigators aim to find predictors of a favourable response to NIV. It is known, from clinical practice and from studies, that not all patients respond favourably. Until now, data have shown that patients with CHRF benefit. Furthermore, benefits at least in terms of improvement in gas exchange, seem to be more prominent in patients with severe stable hypercapnia. In contrast, our group has shown that patients that remain hypercapnic after an exacerbation do not uniformly benefit. An individual COPD phenotype benefiting most from this demanding therapy has not been identified.
The aim of the present study is to investigate whether home initiation of chronic NIV in stable COPD patients with CHRF is non-inferior to inpatient initiation in terms of improvement in PaCO2 after 6 months.
Secondary outcomes are change in lung function (forced expiratory volume in 1 second (FEV1), lung volumes (total lung capacity (TLC), residual volume (RV) and RV%TLC), and diffusion capacity (DLCO (%predicted)), change in HRQoL, and costs including cost-effectiveness analyses.
The secondary objective of the study is to collect patient demographics (age, weight, height, social status, HRQoL, anxiety and depression scores, data on comorbidities and medication use), respiratory function (lung function as well as measures of respiratory muscle activity, arterial blood gases), and inflammatory blood markers, in order to analyse how differences in baseline parameters are related to changes in HRQoL.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Home initiation | Experimental | Device: Transcutaneous measurements of PCO2, Device: Telemonitoring, Device: EMG, Other: Home initiation of NIVHome initiation of long-term NIV will be compared with standard in-hospital initiation. NIV at home will be titrated by a specialised nurse of our home mechanical ventilation centre (HMV) on transcutaneously measured gas exchange and respiratory electromyography and will be adjusted with the use of telemedicine. |
| Inhospital initiation | Active comparator | Device: Transcutaneous measurements of PCO2, Device: EMG, Other: Inhospital initiation of NIVInhospital initiation of NIV is standard care and in the study will be set as the control arm. |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (3 listed)
- Indication to initiate chronic NIV in COPD patients (GOLD stage III or IV: FEV1/ forced vital capacity (FVC)< 70% and FEV1< 50% predicted; PaCO2 > 6.0 kPa in stable condition, which means no COPD exacerbation for 4 weeks and a pH > 7.35)
- Age > 18 years
- Existence of a sufficient social support network making initiation of HMV at home possible and safe.
Key exclusion criteria (2 listed)
- Instable severe cardiac comorbidities (left ventricular ejection fraction below 45%, instable angina pectoris complaints)
- Patients admitted to a nursing home
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 |
|---|---|---|
| Transcutaneous measurements of PCO2PCO2 will be measured transcutaneously with an ear lobe sensor before initiation of NIV, and during the initiation period (SenTec DM®, Software V-STATS 4.0; SenTec AG; Therwil, Switzerland) | Device | Home initiation, Inhospital initiation |
| TelemonitoringTelemonitoring will be used to send data from the transcutaneous measurements, data from the EMG measurements and data from the ventilator from home to the hospital. | Device | Home initiation |
| EMGSurface EMG of the respiratory muscles will be used to monit patients in both groups as a surrogate marker of respiratory muscle unloading and to detect PVA during NIV | Device | Home initiation, Inhospital initiation |
| Home initiation of NIVThe primary aim of the study is to compare home and inhospital initiation of NIV | Other | Home initiation |
| Inhospital initiation of NIVThe primary aim of the study is to compare home and inhospital initiation of NIV | Other | Inhospital initiation |
Primary outcome
Change in daytime PaCO2
Time frame: Baseline, 6 months
An arterial function will be performed during spontaneous breathing without oxygen after 6 months.
9 secondary outcomes
Change in FEV1
Time frame: Baseline, 6 months
Change in health-related quality of life (HRQoL)
Time frame: Baseline, 6 months
Incremental cost-utility ratio
Time frame: Baseline, 6 months
Number of participants with treatment-related adverse events
Time frame: Baseline, 3 months and 6 months
Compliance
Time frame: Baseline, 3 months and 6 months
Change in exercise tolerance
Time frame: Baseline, 6 months
Change in hyperinflation
Time frame: Baseline, 6 months
Change in diffusion capacity
Time frame: Baseline, 6 months
Change in PaCO2
Time frame: Baseline, 3 months
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 17 Dec 2018.
- Derived from this study: PubMed 31484786Duiverman ML, Vonk JM, Bladder G, van Melle JP, Nieuwenhuis J, Hazenberg A, Kerstjens HAM, van Boven JFM, Wijkstra PJ. Home initiation of chronic non-invasive ventilation in COPD patients with chronic hypercapnic respiratory failure: a randomised controlled trial. Thorax. 2020 Mar;75(3):244-252. doi: 10.1136/thoraxjnl-2019-213303. Epub 2019 Sep 4.
- Individual participant dataSharing planned: No
Related trials for Chronic Obstructive Pulmonary Disease
Active, not recruiting
Symptoms and Functions in Patients With COPD and Chronic Bronchitis Switching From CIG to THS
COPD, Smoking
Not yet recruitingPhase 2/3
An Open-Label Extension Study to Evaluate Inhaled Treprostinil SMI in Participants With Pulmonary Hypertension Associated With Chronic Obstructive Pulmonary Disease (PH-COPD)
Pulmonary Hypertension Associated With Chronic Obstructive Pulmonary Disease
Not yet recruiting
The Aim of the Study is to Decipher the Alterations in Signalling Pathways of Skeletal Muscle Stem Cells (Satellite Cells (SCs)) in Individuals With COPD, as Well as to Examine the Effect of Exercise Training on SCs.
COPD (Chronic Obstructive Pulmonary Disease), Sarcopenia in Elderly
Not yet recruitingPhase 2
Study of Treprostinil Administered Via Soft Mist Inhaler (SMI) in Participants With Pulmonary Hypertension Associated With Chronic Obstructive Pulmonary Disease (PH-COPD)
Pulmonary Hypertension Associated With Chronic Obstructive Pulmonary Disease
RecruitingPhase 3
A Study to Investigate the Efficacy and Safety of Belumosudil Compared With Best Available Therapy in Participants Aged 12 Years or Older With Chronic Graft-versus-host Disease
Chronic Graft Versus Host Disease
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.
Marieke Duiverman, MD PhD principal investigator
University Medical Center Groningen
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Transcutaneous measurements of PCO2, Telemonitoring and EMG in people with Chronic Obstructive Pulmonary Disease, run by University Medical Center Groningen at 1 site in Netherlands.
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 3 inclusion and 2 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 17 Dec 2018. 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 Netherlands. 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?
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 daytime PaCO2 (time frame: Baseline, 6 months). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT02652559, which also lists 1 linked publication.
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 17 Dec 2018; AzTrials last refreshed its copy on 6 Nov 2026.