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Initiation of Home Mechanical Ventilation at Home in Patients With Chronic Hypercapnic Respiratory Failure (Homerun)

Primary Purpose

Respiratory Therapy, Respiration, Artificial, Positive-Pressure Respiration

Status
Completed
Phase
Not Applicable
Locations
Netherlands
Study Type
Interventional
Intervention
Initiation of mechanical ventilation
Sponsored by
University Medical Center Groningen
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Respiratory Therapy

Eligibility Criteria

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

Inclusion Criteria:

  • Indication to initiate non-invasive ventilatory support in patients with a neuromuscular disease or thoracic cage abnormality who suffer from complaints of alveolar hypoventilation (fatigue, headache of dyspnoea) combined with all following elements:
  • arterial carbon dioxide > 6.0 kPa daytime or arterial or transcutaneous carbon dioxide > 6.0 kPa at night or orthopnea as a result of diaphragm paralysis
  • Age > 18 years
  • Existence, of a sufficient network (social or professional) according to the supervising HMV center making initiation of HMV at home possible and safe.

Exclusion Criteria:

  • Patients who already have had HMV due to acute respiratory failure
  • Necessity for invasive ventilatory support
  • Patients admitted to a nursing home

Sites / Locations

  • University Medical Center Groningen

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Hospital initiation

Home initiation

Arm Description

Initiation of mechanical ventilation in hospital initiation of Home Mechanical ventilation takes place in a hospital; this makes this arm the standard care.

Initiation of mechanical ventilation at home Initiation of mechanical ventilation in a patient's home setting with telemonitoring

Outcomes

Primary Outcome Measures

Daytime arterial carbon dioxide
Daytime arterial carbon dioxide (PaCO2) assessed without oxygen supplementation and ventilatory support while the patient is in sitting position

Secondary Outcome Measures

Quality of life
Health related quality of life by using the following questionnaires: SF 36, MRF 28, HADS, SRI
Lung function
evaluate lungfunction in time; with measurments of flow/volume in a sitting and horizontal position
Nocturnal transcutaneous carbon dioxide and saturation
Nocturnal transcutaneous carbon dioxide and saturation in time
costs
evaluation of the costs during initiation and the follow-up for 6 months. This will be objective by using the EuroQol (EQ-5D) questionnaire

Full Information

First Posted
February 17, 2017
Last Updated
June 15, 2018
Sponsor
University Medical Center Groningen
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1. Study Identification

Unique Protocol Identification Number
NCT03203577
Brief Title
Initiation of Home Mechanical Ventilation at Home in Patients With Chronic Hypercapnic Respiratory Failure
Acronym
Homerun
Official Title
Initiation of Home Mechanical Ventilation at Home in a Selectve Group of Patients With Chronic Hypercapnic Respiratory Failure in the Netherlands
Study Type
Interventional

2. Study Status

Record Verification Date
June 2018
Overall Recruitment Status
Completed
Study Start Date
July 2015 (undefined)
Primary Completion Date
December 2017 (Actual)
Study Completion Date
May 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University Medical Center Groningen

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Objective: To prove that initiation of chronic ventilatory support at home, in patients with chronic hypercapnic respiratory failure due to neuromuscular disease (NMD) or thoracic cage problem is not inferior compared to initiation in a hospital based setting. In addition we believe that the start at home is cheaper compared to an in-hospital start. Hypothesis: Initiation of chronic ventilatory support at home is effective, safe and cost effective compared to a hospital-based initiation. Study design: A nationwide non-inferiority multi-center randomized parallel active control study. Study population: Patients with chronic respiratory insufficiency due to a neuromuscular disease (NMD) or thoracic cage problem who are referred for chronic ventilator support. Intervention: The start of HMV at home Standard intervention to be compared to: The start of HMV is normally in a clinical setting as recommended in the national guideline. Outcome measures: Primary: PaCO2. Secondary: Health related quality of life; lung function; nocturnal transcutaneous carbon dioxide assessment and saturation, and costs Sample size calculation/data analysis: This is a non-inferiority trial based on PaCO2 as primary outcome. A difference in favor of the hospital care group of smaller than 0.5 kPa will be labeled as non-inferior. To retain 72 evaluable patients, and allow for drop-outs, we will include 96 patients in total. Cost-effectiveness analysis: A cost analysis will be conducted alongside the clinical trial. Costs of the initiation of HMV at home and in the hospital will be estimated form a societal perspective over a time horizon of 6 months. Time schedule: After an initial phase of 6 months recruitment will start and will take 24 months. Thirty-six months after the start of the study the last assessments will be done and analysis and writing of the papers will start. After 42 months the study will end.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Respiratory Therapy, Respiration, Artificial, Positive-Pressure Respiration, Neuromuscular Diseases, Noninvasive Ventilation, Cost-Benefit Analysis, Ambulatory Monitoring

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
96 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Hospital initiation
Arm Type
Active Comparator
Arm Description
Initiation of mechanical ventilation in hospital initiation of Home Mechanical ventilation takes place in a hospital; this makes this arm the standard care.
Arm Title
Home initiation
Arm Type
Experimental
Arm Description
Initiation of mechanical ventilation at home Initiation of mechanical ventilation in a patient's home setting with telemonitoring
Intervention Type
Procedure
Intervention Name(s)
Initiation of mechanical ventilation
Other Intervention Name(s)
start of home mechanical ventialtion with telemonitoring
Intervention Description
In patient with chronic respiratory insufficient chronic mechanical ventilation will be initiated in the patient his/her setting.
Primary Outcome Measure Information:
Title
Daytime arterial carbon dioxide
Description
Daytime arterial carbon dioxide (PaCO2) assessed without oxygen supplementation and ventilatory support while the patient is in sitting position
Time Frame
6 months after initiation of mechanical ventilation
Secondary Outcome Measure Information:
Title
Quality of life
Description
Health related quality of life by using the following questionnaires: SF 36, MRF 28, HADS, SRI
Time Frame
6 months after initiation of mechanical ventilation
Title
Lung function
Description
evaluate lungfunction in time; with measurments of flow/volume in a sitting and horizontal position
Time Frame
6 months after initation of mechanical ventilation
Title
Nocturnal transcutaneous carbon dioxide and saturation
Description
Nocturnal transcutaneous carbon dioxide and saturation in time
Time Frame
6 months after initiation of mechanical ventilation
Title
costs
Description
evaluation of the costs during initiation and the follow-up for 6 months. This will be objective by using the EuroQol (EQ-5D) questionnaire
Time Frame
6 months after initiation of mechanical ventilation

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Indication to initiate non-invasive ventilatory support in patients with a neuromuscular disease or thoracic cage abnormality who suffer from complaints of alveolar hypoventilation (fatigue, headache of dyspnoea) combined with all following elements: arterial carbon dioxide > 6.0 kPa daytime or arterial or transcutaneous carbon dioxide > 6.0 kPa at night or orthopnea as a result of diaphragm paralysis Age > 18 years Existence, of a sufficient network (social or professional) according to the supervising HMV center making initiation of HMV at home possible and safe. Exclusion Criteria: Patients who already have had HMV due to acute respiratory failure Necessity for invasive ventilatory support Patients admitted to a nursing home
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
P.J. Wijkstra, Prof.
Organizational Affiliation
University Medical Center Groningen
Official's Role
Principal Investigator
Facility Information:
Facility Name
University Medical Center Groningen
City
Groningen
ZIP/Postal Code
9700 RB
Country
Netherlands

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
32682770
Citation
van den Biggelaar RJM, Hazenberg A, Cobben NAM, Gaytant MA, Vermeulen KM, Wijkstra PJ. A Randomized Trial of Initiation of Chronic Noninvasive Mechanical Ventilation at Home vs In-Hospital in Patients With Neuromuscular Disease and Thoracic Cage Disorder: The Dutch Homerun Trial. Chest. 2020 Dec;158(6):2493-2501. doi: 10.1016/j.chest.2020.07.007. Epub 2020 Jul 16.
Results Reference
derived

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Initiation of Home Mechanical Ventilation at Home in Patients With Chronic Hypercapnic Respiratory Failure

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