AzTrials
AzTrials

Respiratory MuscleResPETNCT05234099

Sensitivity and Reproducibility of 18F-fluorodeoxyglucose Positron Emission Tomography for Assessment of Respiratory Muscle Activity

A study testing 18F-FDG Positron emission tomography - MRI, Multiparametric ultrasound imaging and Surface electromyography in people with Respiratory Muscle, run by Institut de Myologie, France at 2 sites in France.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
Search all trials

Trial summary

The assessment of respiratory muscle function is critical within both clinical and research settings. Tools for the assessment of respiratory muscle function are especially useful in diagnosing, phenotyping, understanding pathophysiology, and assessing treatment responses in patients with respiratory symptoms… Read more about this study

Who is it for?
Ages 18 years and olderHealthy volunteers can take part
Conditions the study is for
Respiratory Muscle
What is being tested?
18F-FDG Positron emission tomography - MRI, Multiparametric ultrasound imaging and Surface electromyography
Type of treatment
Injection or infusion
Could I receive a placebo?
No, everyone receives an active treatment
How many people
15 participants
Where
2 sitesFrance
Study dates
5 May 2022to 22 Dec 2023
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
  • Healthy volunteers accepted
  • Adult, Older adult

Who may be able to join

  • Age > 18 yo
  • Non-smoker
  • Signed informed consent
  • Affiliate or beneficiary of a social security scheme
  • Non-Inclusion Criteria:
  • Pregnant or breastfeeding women
Show all 14Show fewer
  • Respiratory, cardiovascular, metabolic, neuromuscular pathologies
  • Claustrophobia
  • Belonephobia
  • Latex allergy
  • Persons subject to a legal protection measure or unable to express their consent
  • Contraindications to MRI (claustrophobia, metal implants)
  • Inability to participate in the study
  • Inability to comply with protocol requirements

Who cannot join

  • Blood sugar> 1.8 g / L (V1, V2, V3)
  • Impossibility of inserting the esophageal and / or gastric tubes (V2, V3)

Trial locations and contacts

2 sites in 1 country.

France2 sites
  • Service hospitalier Fréderic Joliot

    Orsay, 91400

  • Association Institut de Myologie

    Paris, 75013

Other trials in France

About this study

Official title: Evaluation of the Sensitivity and Reproducibility of 18F-fluorodeoxyglucose Positron Emission Tomography Coupled With Magnetic Resonance Imaging for the Assessment of Respiratory Muscle Activity and Relationships With Multiparametric Respiratory Muscle Ultrasound

The assessment of respiratory muscle function is critical within both clinical and research settings. Tools for the assessment of respiratory muscle function are especially useful in diagnosing, phenotyping, understanding pathophysiology, and assessing treatment responses in patients with respiratory symptoms, including critically hill patients and patients with respiratory and/or neuromuscular diseases. Respiratory muscle function is most commonly assessed using flow (i.e. spirometry) and pressure measurements during spontaneous ventilation, voluntary respiratory efforts, or artificially evoked responses using magnetic or electrical stimulation. Some of these approaches may be limited within patients suffering from neuromuscular diseases. The study hypothesis is the 18F-FDG PET technology, heavily used for clinical oncology purposes (diagnostic, staging, response to treatment, prognosis), could be an interesting alternative to invasive measurement of the respiratory muscle activity. In addition, it may contribute to further validate metrics based on multiparametric ultrasound imaging.

Read the detailed description

The assessment of respiratory muscle function is critical within both clinical and research settings. Tools for the assessment of respiratory muscle function are especially useful in diagnosing, phenotyping, understanding pathophysiology, and assessing treatment responses in patients with respiratory symptoms, including critically hill patients and patients with respiratory and/or neuromuscular diseases. Respiratory muscle function is most commonly assessed using flow (i.e. spirometry) and pressure measurements during spontaneous ventilation, voluntary respiratory efforts, or artificially evoked responses using magnetic or electrical stimulation. Some of these approaches may be limited, for instance, when facial muscle weakness occurs and/or when glottis function is compromised, for example in patients with bulbar amyotrophic lateral sclerosis or myopathies. Consequently, widely used respiratory measures can be poor predictors of respiratory muscle alterations and this may contribute to affect clinical decisions such as the time when non-invasive ventilation should be initiated within the disease continuum.

Positron emission tomography (PET) is a nuclear medicine procedure based on the measurement of positron emission from radiolabeled tracer molecules. These radiotracers allow biologic processes to be measured and whole-body images to be obtained which demonstrates sites of radiotracer accumulation. Fluorodeoxyglucose (18F-FDG) is a radiolabeled glucose molecule and is the most common radiotracer used in clinical practice. 18F-FDG PET is most frequently coupled with computed tomography but may also be coupled with magnetic resonance imaging (18F-FDG PET-MRI). 18F-FDG PET is heavily used for clinical oncology purposes (diagnostic, staging, response to treatment, prognosis). 18F-FDG PET also finds applications in other fields for detecting infections and inflammatory processes. 18F-FDG may also be used in muscles that are major user of glucose. 18F-FDG PET offers the opportunity to assess the patterns and work amount of multiple muscles simultaneously, providing a global view of the muscles involved in the realization of a motor task, as previously demonstrated in shoulder muscles.

Ultrasound imaging (US) is attracting a growing interest for the assessment of respiratory muscle function, as it allows bedside and non-invasive assessments. Recently, new US techniques such as shear wave elastography (SWE) have shown promises for the assessment of respiratory muscle work. However, the ability of variables derived from respiratory muscle US to reflect increased muscle work remains unclear. Hence, building evidences supporting non-invasive US biomarkers for respiratory muscle function is necessary.

18F-FDG PET offers a unique opportunity to investigate patterns and work amount of the respiratory muscles. In a resting state, 18F-FDG uptake in the respiratory muscle is known to be small. However, and to the best of our knowledge, 18F-FDG uptake of the respiratory muscles at rest in healthy subjects has never been specifically reported. It is unclear whether 18F-FDG PET may be used to monitor changes in respiratory muscle activity within the disease continuum or in response to an intervention such as the initiation of non-invasive ventilation. The reproducibility of increase 18F-FDG uptake of the respiratory muscles induced remains to be assessed and is a prerequisite to determine its sensitivity to change. Moreover, the relationship between increase 18F-FDG uptake and respiratory muscle work as assessed using other methods (e.g. flow and pressure measurements, surface electromyography (sEMG)) and variables derived from multiparametric US remains to be determined. Since MRI does not use ionizing radiations, and because of very higher soft-tissue contrast capabilities, combining PET to MRI instead of CT is of better relevance for our PET muscular analyses purpose.

Being tested
18F-FDG Positron emission tomography - MRI, Multiparametric ultrasound imaging, Surface electromyography, Transdiaphragmatic preasure measurmement, Magnetic stimulation of the phrenic nerves

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • 18F-FDG Positron emission tomography - MRIDiagnostic test

    All the examinations will be performed in the supine position on the same integrated 3T PET-MRI scanner

  • Multiparametric ultrasound imagingDiagnostic test

    Acquisitions of respiratory muscles (diaphragm, intercostal muscles) will be performed using two 6 MHz central frequency linear transducer (SL 10-2) driven by two identical ultrafast ultrasound devices.

  • Surface electromyographyDiagnostic test

    Also called sEMG

    sEMG recordings will be performed in the left side on the sternocleidomastoid muscle, the intercostal parasternal muscle, and the external oblique muscle using pairs of 20-mm-diameter silver chloride surface electrodes.

  • Transdiaphragmatic preasure measurmementDiagnostic test

    Also called Internal respiratory pressures measurements

    Esophageal and gastric pressures will be measured using 8-cm balloon-catheters.

  • Magnetic stimulation of the phrenic nervesDiagnostic test

    In order to quantify the contractile fatigue in diaphragm induced by the ventilatory task (described below), we will use bilateral anterior magnetic stimulation of the phrenic nerves using two Magstim 200 stimulator.

  • Ventilation against inspiratory loadingDiagnostic test

    A POWERbreathe KH2 device (POWERbreathe International Ltd) will be connected on the inspiratory side of the two-way valve. Level of inspiratory loading will be randomized in order to produce different amounts of muscle work in each subject.

Study groups in NCT05234099
Study groupRoleWhat they receive
Control subjectsExperimentalVisit 1 (V1) (Duration: 2.5h) * Information, verification of inclusion and exclusion criteria, information note. * Consent form. * Location of the diaphragm and parasternal intercostal muscle using ultrasound. * Measurements at rest (mouth pressures, sEMG, ultrasound imaging). * Injection of 3 MBq/kg of 18F-FDG. * 1h resting period. * 18F-FDG PET-MRI scan. Visit 2 (V2) 3-10 days after V1 (Duration: 3h) * Location of the diaphragm and parasternal intercostal muscle. * Measurements at rest (mouth pressures, sEMG, ultrasound imaging) * Magnetic stimulation of the phrenic nerves * Ventilation against inspiratory loading * Magnetic stimulation of the phrenic nerves * Injection of 3 MBq/kg of 18F-FDG * 1h resting period * 18F-FDG PET-MRI scan Visit 3 (V3) 3-10 days after V2 (Duration: 3h) - Identical to visit 2
Receives: Diagnostic Test: 18F-FDG Positron emission tomography - MRI; Diagnostic Test: Multiparametric ultrasound imaging; Diagnostic Test: Surface electromyography; Diagnostic Test: Transdiaphragmatic preasure measurmement; Diagnostic Test: Magnetic stimulation of the phrenic nerves; Diagnostic Test: Ventilation against inspiratory loading

What is being measured

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

  1. Correlation between multiparametric ultrasound and 18F-FDG PET-MRI during respiratory muscle activity measurement

    Existence of a significant correlation between the variables derived from the multiparametric ultrasound and the work of the respiratory muscles induced by the ventilatory spot assessed by 18F-FDG PET-MRI

    Measured: Through study completion, on average 3 weeks

Secondary outcomes (2)
  1. Significant correlation between measurements of respiratory muscle activity assessed by pressure measurements and increased respiratory muscle work induced by the ventilation against inspiratory loading as assessed by 18F-FDG PET-MRI

    Existence of a significant correlation between measurements of respiratory muscle activity assessed by pressure measurements (esophageal pressure, gastric pressure, transdiaphragmatic pressure) and increased respiratory muscle work induced by the ventilation against inspiratory loading as assessed by 18F-FDG PET-MRI

    Measured: Through study completion, on average 3 weeks

  2. Significant correlation between measures of respiratory muscle activity assessed by sEMG and respiratory muscle work induced by the ventilation against inspiratory loading as assessed by 18F-FDG PET-MRI

    Existence of a significant correlation between measures of respiratory muscle activity assessed by sEMG and respiratory muscle work induced by the ventilation against inspiratory loading as assessed by 18F-FDG PET-MRI

    Measured: Through study completion, on average 3 weeks

Timeline

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

  1. First posted10 Feb 2022
  2. Study start5 May 2022
  3. Primary completion22 Dec 2023
  4. Study completion22 Dec 2023

Resources

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
Diagnosis
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrolment
15 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05234099
Sponsor's protocol ID
ResPET
Acronym
ResPET
Status last verified
Apr 2024
First submitted
1 Feb 2022
Last updated
10 Apr 2024
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

A study testing 18F-FDG Positron emission tomography - MRI, Multiparametric ultrasound imaging and Surface electromyography in people with Respiratory Muscle, run by Institut de Myologie, France at 2 sites in France.

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 14 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 10 Apr 2024. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 2 sites in France. 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?

Correlation between multiparametric ultrasound and 18F-FDG PET-MRI during respiratory muscle activity measurement (time frame: Through study completion, on average 3 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 Apr 2024.

Free account

Log in to keep searching

You’ve used your 3 free searches. AzTrials is free: log in or create a free account to keep searching clinical trials and save the ones you want to follow.

Create a free accountLog in