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Trial record 38 of 669 for:    Recruiting, Not yet recruiting, Available Studies | "Muscular Diseases"

Muscle Recovery Following Aortic Surgery Induced ICUAW. (VARIANCE)

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ClinicalTrials.gov Identifier: NCT03714399
Recruitment Status : Not yet recruiting
First Posted : October 22, 2018
Last Update Posted : October 22, 2018
Sponsor:
Collaborators:
Queen Mary University of London
Barts Charity
Information provided by (Responsible Party):
Barts & The London NHS Trust

Brief Summary:
To identify determinants of 'good and bad recovery' from ICUAW and build knowledge around the timing of these processes. Also, the investigators want to discover the effects of ICUAW on physical function and HRQoL after aortic surgery.

Condition or disease
Aortic Diseases Intensive Care Unit Syndrome Intensive Care Neuropathy Intensive Care (ICU) Myopathy Critical Illness Myopathy Surgery

Detailed Description:

The aim is to identify determinants of recovery from intensive care unit-acquired weakness (ICUAW) and to discover the effects of ICUAW on physical function and health-related quality of life (HRQoL) after critical illness. This phenomenon has become more evident over recent years and still requires extensive research that will benefit the patients' quality of life and reduce ICU and hospital length of stay.

ICUAW is an umbrella term for more specifically polyneuropathy and myopathy. Recent research has found that 50% of patients undergoing elective cardiac surgery lose significant muscle mass (9.6% in the wasters group) within the first seven days. These patients are receiving relatively uncomplicated surgery yet still suffering from muscle breakdown, which cannot be described by inactivity alone. ICUAW can lead to a significant increase in mortality, morbidity, hospital-acquired infections and pressure ulcers. Risk factors for ICUAW include neuromuscular blocking agents, hyperglycaemia, inactivity and sepsis. The correlation between a relatively homogenous (cardiac surgical) group and patient-centred outcomes during recovery such as functional ability and health-related quality of life (HRQoL) has been little studied.

Patients undergoing elective aortic surgery at St Bartholomew's Hospital will aim to be recruited for the study. We have chosen the cardiac surgical model due to being a homogenous cohort where the time of insult from surgery from the potential cardiac bypass, can be measured in correlation with ICUAW. Due to the clamped aorta within the operation, prolonged periods of reduced blood flow to the body occurs, and therefore an element of ischaemia and reperfusion can lead to muscle wasting. Rectus Femoris cross-sectional area (RFcsa) will be measured when the patient attends the pre-assessment clinic, on day 7, day 15/hospital discharge and the six week and 3-month outpatient clinic. To assess and quantify 'good recovery,' we will correlate these tests with functional capacity and HRQoL. Additionally, Blood samples and urine samples will be taken at pre-defined intervals before and during the patients' admission to critical care. The blood samples will observe markers of oxidative stress and organ injury along with molecular profiles. A muscle biopsy will be taken during surgery and observed for histological and fibre profiles. VARIANCE is an observational study attempting to understand the recovery of muscle, strength and HRQoL over time.

The primary Objective is to identify determinants of recovery from ICUAW and to discover the effects of ICUAW on physical function and health-related quality of life (HRQoL) after aortic surgery. Precisely, to observe the cross-sectional area of the Rectus Femoris (RFcsa) and correlate this with muscle strength and HRQoL during the recovery phase. The cross-sectional area of the Rectus Femoris (RFcsa), hand-held dynamometry, knee straightening dynamometry, Free Fat Mass Index, standing and lying vital capacity, MRC-SS score, short physical performance battery will be observed. Also, HRQoL will be measured using the RNLI (reintegration to normal living index), HADS (hospital and anxiety depression score, EQ-5D-5L (EuroQol research foundation). The primary endpoint will be once all these data are gathered and analysed.

The secondary aim is to understand the molecular and genomic profile of blood samples and the histology of the muscle biopsies. The secondary objective will be supported with additional data from urine analysis (Albumin-creatinine ratio, ACR). The secondary endpoint will be once these data are gathered and analysed.


Study Type : Observational
Estimated Enrollment : 100 participants
Observational Model: Cohort
Time Perspective: Prospective
Official Title: A Prospective Observational Study Into Muscle Recovery Following Aortic Surgery Induced Intensive Care Unit-acquired Weakness (VARIANCE).
Estimated Study Start Date : December 1, 2018
Estimated Primary Completion Date : August 1, 2020
Estimated Study Completion Date : August 1, 2020

Group/Cohort
ICUAW group
The physical and psychological effects of ICUAW on patients undergoing aortic valvular surgery will be observed. Physical function and HRQoL will be analysed and correlated with RFcsa. Additionally, biological markers will be used to understand molecular and genomic profiles.



Primary Outcome Measures :
  1. To observe the change in cross sectional area of the Rectus Femoris (RFcsa) during critical illness and recovery. [ Time Frame: Pre-operatively, day 7, Hospital Discharge approximately 14 days, 6-9week follow up clinic and 3-month follow up clinic. ]
    RFcsa will be calculated using B-mode ultrasound (US) at pre-determined time points. Additionally, the images acquired will have histogram analysis in adobe photoshop software. The RFcsa will be correlated with indices of muscle strength and HRQoL.

  2. To Observe a change in Hand Held Dynamometry strength (grip strength) and correlate this with RFcsa, function and HRQoL during critical illness and recovery. [ Time Frame: Pre-operatively, Day 7, Hospital Discharge approximately 14 days, 6-9 week follow up clinic, 3 month +/- 4 weeks follow up clinic ]
    Hand-held dynamometry will be calculated using the JAMAR hand-held hydraulic dynamometer. We will assess both hands and take the mean of 3 trials, producing a maximal grip result.

  3. To observe a change in Knee straightening dynamometry, strength and joint moment (torque) and correlate this with RFcsa, function and HRQoL during critical illness and recovery. [ Time Frame: Pre-operatively, Day 7, Hospital Discharge approximately 14 days, 6-9 week follow up clinic, 3 month +/- 4 weeks follow up clinic ]
    The test will be conducted using a Lafayette Manual Muscle Tester. Joint knee moment (torque) and strength will be measured.

  4. To test the Medical Research Council Sum Score (MRC-SS). MRC-SS measures global strength and ambulation. [ Time Frame: Day 7 ]
    This test will be conducted once to reaffirm whether patients' have ICUAW. A score can range from 0 (paralysis) to 60 (normal strength). A score of less than 48 indicates the patient has ICUAW. Therefore, a lower score is associated with worse outcomes.

  5. To observe a change in Short Physical Performance Battery (SPPB) and correlate this with RFcsa, function and HRQoL during critical illness and recovery. [ Time Frame: Pre-operatively, Day 7, Hospital Discharge approximately 14 days, 6-9 week follow up clinic, 3 month +/- 4 weeks follow up clinic. ]
    SPPB will be measured at similar time points to understand a patients' functional status.

  6. Lying and Standing Vital Capacity (FVC - forced vital capacity) and correlate this with RFcsa, function and HRQoL during critical illness and recovery. [ Time Frame: Pre-operatively, Day 7, Hospital Discharge approximately 14 days, 6-9 week follow up clinic, 3 month +/- 4 weeks follow up clinic ]
    Lying and standing vital capacity will be measured using a hand held spirometer.

  7. To measure Free Fat Mass Index (FFMI) and correlate this with RFcsa, function and HRQoL during critical illness and recovery. [ Time Frame: Pre-operatively, Day 7, Hospital Discharge approximately 14 days, 6-9 week follow up clinic, 3 month +/- 4 weeks follow up clinic. ]
    Free fat mass index (FFMI) and free fat mass (FFM) will be measured using the bodystat 1500 device. Other values will also be recorded from the test including body fat percentage and lean mass percentage. The body stat 1500 is an electrical device that uses electrical impedance to obtain results (objective data).

  8. To measure the EQ-5D-5L (Euroscore) to assess general health and correlate this with the primary objective (RFcsa). [ Time Frame: Pre operatively, Day 7, Hospital discharge approximately 14 days, 6-9 week follow up and 3 month +/- 4 weeks follow up. ]
    EQ5D-5L is a standardised tool that provides a simple generic measure of health. A summation of all the levels will be converted to a single index value using the EQ5D-5L crosswalk index value calculator. The general health score can range from 0 (worst health imaginable) to 100 (best health imaginable).

  9. Hospital anxiety and depression score (HADS) to assess HRQoL and correlate this with the overall primary objective (RFcsa). [ Time Frame: Pre-operatively, Day 7, Hospital discharge approximately 14 days, 6-9 week follow up and 3 months +/- 4 weeks. ]
    The HADS is an assessment that measures whether a patients is suffering from anxiety or depression. HADS is a self assessment consisting of 16 items. A result of between 0 and 7 indicates a normal case, between 8 and 10 indicates borderline abnormal and between 11 and 21 indicates abnormal levels of anxiety and depression.

  10. Reintegration to normal living index (RNLI) to assess HRQoL and correlate this with the overall primary objective (RFcsa). [ Time Frame: Pre-operatively, 6-9 week follow up and 3 month +/- 4 weeks. ]
    The RNLI is a 5 domain 11-tool item aimed at assessing the degree to which patients' who have experiences traumatic and incapacitating illness achieve reintegration into society. The RNLI score is based out of 110, which will be proportionally converted to create a score of 100. Zero indicates no integration whereas 100 implies full integration.


Secondary Outcome Measures :
  1. The secondary aim is to understand the molecular profile (bloods). [ Time Frame: Pre-operatively, Day 1, Day 3, Day 7, hospital discharge approximately 14 days, 6-9 week follow up and 3-months +/- 4 weeks follow up. ]
    Blood analysis will contain and analyse but not limited to markers of oxidative stress injury, inflammation, MiRNA and injury to multiple organs will be quantified. We will store Buffy coat and plasma to understand these profiles.

  2. Urine Analysis [ Time Frame: pre-operatively, Day 1, Day 3, Day 7, hospital discharge approximately 14 days, 6-9 week follow up and 3-months +/- 4 weeks follow up. ]
    Urine analysis observes albumin-creatinine ratio (ACR)

  3. Muscle Biopsy [ Time Frame: Intra-operatively ]
    A muscle biopsy will be taken from patients whilst under anaesthesia. The biopsy observes pathways relevant to muscle homeostasis using biochemical and molecular techniques.

  4. Cardiac post operative morbidity score (C-POMS) will be used to calculate morbidity risk. [ Time Frame: Day 3, day 5, day 8 and day 15 post cardiac surgery. ]
    C-POMS is additional data that will be collected and analysed. C-POMS is a validated tool assessing in-hospital morbidity burden (score 0-13) derived by noting the presence of 13 morbidity domains on days 3, 5, 8 and 15 after surgery. A higher score indicates a greater morbidity burden.


Biospecimen Retention:   Samples With DNA
Muscle biopsies taken from the thigh and chest wall will be taken at the time of surgery for histological analysis. Blood samples (plasma and buffy coat) will also be taken for mediators and markers of oxidative stress injury (e.g. 8-isoprostane), inflammation (e.g. interleukin-6 and soluble tumour necrosis factor receptor) and injury to multiple organs will be quantified. Urine will be used to measure albumin-creatinine ratio (ACR) as a marker of endothelial injury.


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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
Inclusion criteria include any consenting adult receiving elective aortic surgery at Bartshealth NHS trust with no evidence of pre-hospital neuromuscular conditions.
Criteria

Inclusion Criteria:

  • Above the age of 18
  • Receiving elective aortic valvular surgery at Barts Health NHS Trust

Exclusion Criteria:

  • Previous Stroke
  • Neuromuscular disease
  • Malignancy
  • Underlying neuromuscular disease
  • Paediatrics
  • Non-consenting adults

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03714399


Contacts
Contact: Mark Griifiths, PhD FRRCP 07875999126 Mark.Griffiths@bartshealth.nhs.uk
Contact: Ashley Thomas, MSc 07597875857 ashleythomas@nhs.net

Locations
United Kingdom
St Bartholomew's hospital (Barts NHS trust) Not yet recruiting
London, United Kingdom, EC1A 7BE
Contact: Griffiths, Mark Griffiths, FRRCP, PhD    447875999126    Mark.Griffiths@bartshealth.nhs.uk   
Principal Investigator: Mark Griffiths, FRRCP, PhD         
Sponsors and Collaborators
Barts & The London NHS Trust
Queen Mary University of London
Barts Charity
Investigators
Principal Investigator: Mark Grffiths, FRRCP, PhD Substantive Employee and primary supervisor to PhD student
Principal Investigator: Julie Sanders, MSc, PhD Director of research and supervisor to PhD student
Principal Investigator: Ashley Thomas, MSc Substantive employee and PhD student

Publications:
Responsible Party: Barts & The London NHS Trust
ClinicalTrials.gov Identifier: NCT03714399     History of Changes
Other Study ID Numbers: 012396 (VARIANCE)
First Posted: October 22, 2018    Key Record Dates
Last Update Posted: October 22, 2018
Last Verified: April 2018
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No

Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No

Keywords provided by Barts & The London NHS Trust:
Intensive Care Unit Acquired Weakness (ICUAW)
Critical Illness Polyneuromyopathy (CIPM)
Health Related Quality of Life (HRQoL)
Ultrasound (US)
Cardiac Surgery
Rectus Femoris Cross Sectional Area (RFcsa)

Additional relevant MeSH terms:
Critical Illness
Muscular Diseases
Aortic Diseases
Disease Attributes
Pathologic Processes
Musculoskeletal Diseases
Neuromuscular Diseases
Nervous System Diseases
Vascular Diseases
Cardiovascular Diseases