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Upright MRI in lung disease

Upright magnetic resonance imaging in COPD and diaphragm disease

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ISRCTN
Registry ID
ISRCTN15470049
Enrollment
80
Registered
2018-05-23
Start date
2018-06-01
Completion date
Unknown
Last updated
2021-05-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Diaphragmatic weakness or COPD (chronic obstructive pulmonary disease) with hyperinflation Respiratory

Interventions

All participants (healthy individuals and patients) will undergo the following tests/procedures: 1. Relevant Past Medical History Including medication history & smoking status.

Sponsors

University of Nottingham
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Healthy volunteers and patients with diaphragm weakness (due to neuromuscular disease, e.g. motor neuron disease, and non-neuromuscular disease e.g. trauma) and patient with COPD with hyperinflation General inclusion criteria: 1. Adult - male or female, aged 18 to 90 years old 2. Capacity to give informed consent 3. Able to hold their breath for 10 seconds 4. Able to understand the requirements of the study and to cooperate with the study procedures Cohort-specific inclusion criteria: Healthy participants: 1. No reported or diagnosed chronic respiratory disease COPD with hyperinflation: 1. Evidence of airflow obstruction on spirometry – FEV1/FVC < 0.7 and FEV1 <80% 2. Diagnosis of hyperinflation based on imaging or lung function measures Diaphragm weakness due to non-neuromuscular disease: 1. Established diagnosis of diaphragm weakness due to non-neuromuscular disease, e.g. viral illness, trauma Diaphragm weakness due to neuromuscular disease: 1. Established diagnosis of diaphragm weakness due to neuromuscular disease

Exclusion criteria

Exclusion criteria: 1. Unsuitable for MRI scanning (e.g. have metal implants or pacemaker or contraindicated following questionnaire) 2. Deemed unlikely to comply with instructions during imaging 3. Deemed not fit enough to tolerate procedure 4. Deemed unsuitable by clinical investigator for other reasons 5. History of lung volume reduction procedure

Design outcomes

Primary

MeasureTime frame
1. Change in diaphragm position and morphology caused by a change in posture (vertical to horizontal position or vice versa), measured by analysis of MR images once during the one scan visit. Analysis is performed using Matlab software 2. Degree of impairment in diaphragm movement in COPD patients with hyperinflation, measured once during the one scan visit. Analysis is performed using Matlab software. Patient scans are compared to healthy volunteer scans 3. Correlation between lung function abnormality with abnormalities in diaphragm movement as noted on MRI. Spirometry and scan are performed on the same day during the scan visit

Secondary

MeasureTime frame
Tolerability data on the ability of participants of each group to adhere to the protocol thus informing the study design of future trials. Participants are asked to fill a visual analogue scale for breathless comparing the severity of breathless in lying and seated positions, right after completing the scans

Countries

United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026