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The Intensive Care Muscle imaging study

A pilot observational study to investigate the structure and function of skeletal muscle in survivors of critical illness using magnetic resonance imaging (MRI)

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ISRCTN
Registry ID
ISRCTN17829967
Enrollment
30
Registered
2015-07-08
Start date
2015-06-01
Completion date
Unknown
Last updated
2017-09-04

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

Conditions

Intensive care unit acquired weakness Musculoskeletal Diseases Muscle wasting and atrophy, not elsewhere classified

Interventions

The skeletal muscle of survivors of critical illness will be studied using 3 broad approaches: 1. Magnetic resonance imaging (MRI) 2. 2D ultrasound imaging 3. Clinical assessment (quadricpes dynamome
Medical Research Council sum-score of global muscle strength
6 minute walk test) 4. Blood samples will be drawn for serological analysis

Sponsors

University of Edinburgh
Lead Sponsor
NHS Lothian
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Group 1 (10 patients): 1. Adult ICU survivors 2. Ventilated for 48 hours or more 3. Good level of physical function prior to hospital admission (Rivermead Mobility Index (RMI) >/14 at any time in the week prior to hospital admission) 4. Within 7 days of ICU discharge 5. Evidence of very poor physical recovery (RMI =8) Group 2 (10 patients): 1. Adult ICU survivors 2. Paired by age, gender and body mass index (BMI) to Group 1 3. Ventilated for 48 hours or more 4. Good level of physical function prior to hospital admission (RMI =15 at any time in the week prior to hospital admission) 5. Within 7 days of ICU discharge 6. Evidence of very good physical recovery (RMI = 9) Group 3 (10 patients): 1. A healthy community based sample derived from patients presenting for day case surgery. 2. Paired by age, gender, and BMI to groups 1 and 2 3. Good level of physical function (RMI = 15)

Exclusion criteria

Exclusion criteria: Exclusion criteria for groups 1 and 2: 1. <18 years of age 2. Patient receiving palliative care 3. Patient has a contraindication to MRI imaging 4. Neurological diagnosis 5. Background chronic neuromuscular disease 6. Patient lacks mental capacity 7. Malignancy 8. Chronic inflammatory disease 9. Clinical instability Exclusion criteria for group 3 1. <18 years 2. Malignancy 3. Chronic inflammatory disease 4. Background chronic neuromuscular disease 5. Neurological diagnosis 6. Presenting for lower limb arthroplasty 7. Patient lacks mental capacity

Design outcomes

Primary

MeasureTime frame
For group 1 all measurements will be taken at baseline and 3 months; for groups 2 and 3 all measurements will be taken at baseline only: 1. Quadriceps muscle volume.

Secondary

MeasureTime frame
For group 1 all measurements will be taken at baseline and 3 months; for groups 2 and 3 all measurements will be taken at baseline only: 1. Qualitative assessment of muscle oedema and focal inflammation 2. Relative fat fraction (measured by the three-point Dixon method) 3. Mean elasticity (measured in KPa using magnetic resonance elastography) 4. Quadriceps strength (quadriceps dynamometry)

Countries

United Kingdom

Contacts

Public ContactDawn Campbell

Outcome results

None listed

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