search
Back to results

Mechanical Insufflation -Exsufflation in Children With NMD and Weak Cough

Primary Purpose

Neuromuscular Diseases in Children

Status
Completed
Phase
Not Applicable
Locations
Norway
Study Type
Interventional
Intervention
Symmetric settings (high pressures/fast rate)
Asymmetric settings (Pi<Pe/Ti>Te)
Preinclusion settings
Sponsored by
Oslo University Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Neuromuscular Diseases in Children

Eligibility Criteria

6 Months - 18 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Diagnosed neuromuscular disease < 18 years
  • Established use (> 3mnd) of MI-E.
  • Reduced PCF

    • PCF < 270 l/min (when > 12 years)
    • < 5th percentiles for PCF 16 (when 4 - 12 years)
  • Clinical indication (difficulty to clear secretions, audible weak cough, history of pneumonia or frequent or prolonged respiratory tract infections).

Exclusion Criteria:

  • age < 6 mnd
  • obstructive lung disease (hyperinflation or emphysema on x-ray.

Sites / Locations

  • Helse bergen HF
  • Oslo university hospital
  • Stavanger university hospital
  • St. Olav Trondheim university hospital

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

Sham Comparator

Arm Label

MI-E testing symmetric settings

MI-E testing assymetric settings

Settings in use

Arm Description

Symmetric settings is one of 3 different settings that will be tested on the same day but in randomized order.

Asymmetric settings is one of 3 different settings that will be tested on the same day but in randomized order.

Settings in use is one of 3 different settings that will be tested on the same day but in randomized order

Outcomes

Primary Outcome Measures

PCF in the MI-E circuit
Recording of maximal value produced by the MI-E device during Cough
Patient reported comfort
Comfort rated on a Visual Analog Scale (VAS) (0-100) where 100 is very uncomfortable and 0 is very comfortable.

Secondary Outcome Measures

Carbon dioxide
Transcutaneous trend measurement of CO2 during data collection
Oxygen
Transcutaneous trend measurement of peripheral O2 during data collection
Hart rate
Transcutaneous trend measurement of hart rate during data collection
Patient reported efficacy
Efficacy rated on a Visual Analog Scale (0-100) where 100 is not efficient at all and 0 is very efficient.

Full Information

First Posted
February 4, 2019
Last Updated
January 19, 2023
Sponsor
Oslo University Hospital
search

1. Study Identification

Unique Protocol Identification Number
NCT04081116
Brief Title
Mechanical Insufflation -Exsufflation in Children With NMD and Weak Cough
Official Title
The Optimal Settings of MI-E in Children With NMD and Weak Cough
Study Type
Interventional

2. Study Status

Record Verification Date
January 2023
Overall Recruitment Status
Completed
Study Start Date
January 1, 2019 (Actual)
Primary Completion Date
February 28, 2021 (Actual)
Study Completion Date
February 28, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Oslo University Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Neuromuscular diseases (NMD) in children are severe, possibly life-threatening orphan conditions. The children are vulnerable and often subject to rapid deterioration of pulmonary function due to impaired ability to clear airway secretions. The use of mechanical cough augmentation with insufflation-exsufflation (MIE) is a strategy to treat and prevent. Possible major benefits are described, but optimal settings for best efficacy and comfort in children are not established. The project aim to improve the quality of the treatment with MIE in children with NMD and weak cough. On the basis of a bench study a clinical trial aims to examine the most effective MIE settings when used in stable state and when respiratory tract infections are present.
Detailed Description
On the basis of a prevalence study and a bench study different settings will be studied in children with NMD and weak cough to examine if settings derived from the lung model, are optimal to increase the peak cough flow (PCF) and comfort measured by visual analogue scale (VAS) in children with NMD and weak cough.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Neuromuscular Diseases in Children

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
Three different settings are tested on the same patients but in randomized order.
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Masking Description
Participant, care provider, investigator and outcomes assessor are blinded from the order of the settings tested. Only a technician change settings and know the order.
Allocation
Randomized
Enrollment
77 (Actual)

8. Arms, Groups, and Interventions

Arm Title
MI-E testing symmetric settings
Arm Type
Experimental
Arm Description
Symmetric settings is one of 3 different settings that will be tested on the same day but in randomized order.
Arm Title
MI-E testing assymetric settings
Arm Type
Experimental
Arm Description
Asymmetric settings is one of 3 different settings that will be tested on the same day but in randomized order.
Arm Title
Settings in use
Arm Type
Sham Comparator
Arm Description
Settings in use is one of 3 different settings that will be tested on the same day but in randomized order
Intervention Type
Other
Intervention Name(s)
Symmetric settings (high pressures/fast rate)
Intervention Description
Describes settings on the MI-E device
Intervention Type
Other
Intervention Name(s)
Asymmetric settings (Pi<Pe/Ti>Te)
Intervention Description
Lower insufflation pressures at longer times
Intervention Type
Other
Intervention Name(s)
Preinclusion settings
Intervention Description
Settings in use at start of study
Primary Outcome Measure Information:
Title
PCF in the MI-E circuit
Description
Recording of maximal value produced by the MI-E device during Cough
Time Frame
30 minutes.
Title
Patient reported comfort
Description
Comfort rated on a Visual Analog Scale (VAS) (0-100) where 100 is very uncomfortable and 0 is very comfortable.
Time Frame
Total time use 30 min
Secondary Outcome Measure Information:
Title
Carbon dioxide
Description
Transcutaneous trend measurement of CO2 during data collection
Time Frame
maximal time use is 30 min
Title
Oxygen
Description
Transcutaneous trend measurement of peripheral O2 during data collection
Time Frame
maximal time use is 30 min
Title
Hart rate
Description
Transcutaneous trend measurement of hart rate during data collection
Time Frame
Total max 30 minutes (During three MI-E trials)
Title
Patient reported efficacy
Description
Efficacy rated on a Visual Analog Scale (0-100) where 100 is not efficient at all and 0 is very efficient.
Time Frame
The VAS is recorded after each of the three trials. Total time use 30 min

10. Eligibility

Sex
All
Minimum Age & Unit of Time
6 Months
Maximum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Diagnosed neuromuscular disease < 18 years Established use (> 3mnd) of MI-E. Reduced PCF PCF < 270 l/min (when > 12 years) < 5th percentiles for PCF 16 (when 4 - 12 years) Clinical indication (difficulty to clear secretions, audible weak cough, history of pneumonia or frequent or prolonged respiratory tract infections). Exclusion Criteria: age < 6 mnd obstructive lung disease (hyperinflation or emphysema on x-ray.
Facility Information:
Facility Name
Helse bergen HF
City
Bergen
Country
Norway
Facility Name
Oslo university hospital
City
Oslo
Country
Norway
Facility Name
Stavanger university hospital
City
Stavanger
Country
Norway
Facility Name
St. Olav Trondheim university hospital
City
Trondheim
Country
Norway

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
33887060
Citation
Morrow B, Argent A, Zampoli M, Human A, Corten L, Toussaint M. Cough augmentation techniques for people with chronic neuromuscular disorders. Cochrane Database Syst Rev. 2021 Apr 22;4(4):CD013170. doi: 10.1002/14651858.CD013170.pub2.
Results Reference
derived

Learn more about this trial

Mechanical Insufflation -Exsufflation in Children With NMD and Weak Cough

We'll reach out to this number within 24 hrs