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Not yet recruiting NCT06404229

Use of CPETarm for Risk Stratification of Patients With CLTI

No phase Interventional Chronic Limb-Threatening Ischemia Surgery-Complications

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: CardioPulmonary Exercise Testing.
Who it may be relevant to
Registry conditions: Chronic Limb-Threatening Ischemia, Surgery-Complications. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United Kingdom
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Novel Use of Bedside Arm Ergometry CardioPulmonary Exercise Tests for the Risk Stratification of Patients With Chronic Limb-threatening Ischaemia: A Feasibility Trial

Overview

This is a prospective cohort study of patients undergoing surgery for chronic limb threatening ischaemia. Prior to surgery, patients will undergo CardioPulmonary Exercise testing (CPET) using an arm ergometer. Feasibility outcome measures will be recorded at testing and participants will be followed up for a period of up to 5 years to obtain clinical outcome measures.

Detailed description

Chronic limb-threatening ischaemia (CLTI) is the most severe clinical manifestation of peripheral arterial disease, defined by the presence of pain at rest and/or tissue loss affecting the legs. It is a major cause of chronic pain, amputation and death. CLTI is a growing global healthcare problem attributable to the ageing population and increase of risk factors such such as diabetes.

Prevalence of high blood pressure, heart disease and diabetes is high amongst this cohort of patients and so it is unsurprising that surgery is associated with an alarmingly high risk of illness, complications and even death when compared to other types of surgery. As nearly half of the patients present as an emergency, assessment and optimisation of health prior to surgery is challenging.

The aims of the assessment prior to surgery includes optimising any current health problems, understanding what care may be required after surgery, allowing the patient to be fully informed of the risks and considering non surgical options where appropriate. Inadequate risk stratification can lead to delays in theatre, increased length of hospital stay and unnecessary loss of limb and/or life.

Currently there is no established method to risk stratify CLTI patients presenting as an emergency. CardioPulmonary Exercise Testing (CPET) is an exercise test useful in identification of a number of heart and lung conditions. The test is established for risk-stratification in other populations but its method of using a bicycle is not suitable for CLTI patients, nor has it previously been used in the emergency setting. This study will assess whether CPET using arm exercise instead of the traditional bicycle is a feasible test that can be performed at the bedside within 48 hours of intention to treat, required to make it a practical test in the assessment of emergency patients.

Hypothesis:

1. Cardiopulmonary exercise testing using an arm ergometer (CPETarm) is a feasible, acceptable and safe tool to use at the 'bedside' in patients undergoing emergency surgery for chronic limb threatening ischaemia (CLTI). 2. Values obtained from CPETarm and/or hand grip strength can be used to predict post operative outcomes including major adverse cardiovascular events and mortality for this group of patients.

Recruitment:

The study will enrol 120 consecutive, eligible and consenting patients admitted with with CLTI to the Manchester Vascular Centre at Manchester University National Health Service Foundation Trust. Patients scheduled to undergo non elective surgical or endovascular treatment of their chronic limb threatening ischaemia will be screened for inclusion. Decision for surgery/management will be recommended by their Consultant Vascular Surgeon.

Interventions

  • Diagnostic test CardioPulmonary Exercise Testing
    CardioPulmonary Exercise Testing using an arm ergometer prior to surgery

Primary outcome measures

  • Acceptability of bedside CPET [Time frame: At time of CPET testing (1 day)]
  • Recruitment rate (uptake of bedside CPET) [Time frame: At time of CPET testing (1 day)]
  • Practicality of bedside CPET [Time frame: At time of CPET testing (1 day)]
  • Patient reported outcome measures [Time frame: 30 days]
  • Adverse or unexpected events report [Time frame: At time of CPET testing (1 day)]
Secondary outcome measures (11)
  • Peri-operative complications [Time frame: Recorded at 30 days]
  • All cause mortality [Time frame: Recorded at 30 days, 90 days, 1 year, 3 years and 5 years]
  • Amputation-free survival [Time frame: Recorded at 30 days, 90 days, 1 year, 3 years and 5 years]
  • Level of care post-surgery [Time frame: Recorded at 30 days]
  • Higher level of care length of stay [Time frame: Recorded at 30 days]
  • Length of hospital stay [Time frame: Recorded at 30 days]
  • Discharge destination [Time frame: Recorded at 30 days]
  • Rate of re-intervention [Time frame: Recorded at 30 day and 90 days]
  • Hospital readmission rate [Time frame: Recorded at 30 and 90 days.]
  • Health related quality of life [Time frame: Recorded at 30 and 90 days]
  • Major adverse cardiovascular events [Time frame: Recorded at 30 and 90 days]

Eligibility criteria

Inclusion criteria

  • Ability and willingness to give written informed consent
  • Diagnosis of chronic limb threatening ischaemia, undergoing one of the following procedures: Infra inguinal bypass, Extra anatomical bypass, Common femoral endarterectomy, Endovascular treatment, Primary amputation

Exclusion criteria

  • Patients with active medical conditions deemed an absolute contraindication for undertaking CPET
  • Ongoing evaluation for coronary artery disease (e.g awaiting stress test or cardiac catheterisation or requiring the up titration of anti anginal medications)
  • Active arrthymic requiring the initiation or up titration of an anti arrthymic medication
  • Active congestive cardiac failure requiring the initiation or up titration of diuretic therapy.
  • Severe cardiac valvular stenosis
  • Physical disability precluding ability to perform CPETarm
  • Psychiatric disorder or dementia precluding them from consenting for research and/or undertaking testing and/or follow up

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
N/A
Model
Single group
Masking
Open label
Primary purpose
Diagnostic

Study locations

United Kingdom · 1 center
  • University of Manchester — Manchester

Publications

  • [1] Conte MS, Bradbury AW, Kolh P, et al. GVG Writing Group for the Joint Guidelines of the Society for Vascular Surgery (SVS), European Society for Vascular Surgery (ESVS), and World Federation of Vascular Societies (WFVS). Global Vascular Guidelines on the Management of Chronic Limb-Threatening Ischemia. Eur J Vasc Endovasc Surg. Eur J Vasc Endovasc Surg, 2019. 58: p. 1-109.
  • [2] Waton S, Johal A, Li Q, et al. National Vascular Registry: 2023 State of the Nation Report. London: The Royal College of Surgeons of England, November 2023.
  • Hodge S, Haque A, Quraishi-Akhtar T, Bryan A, Rogers S, Bowling FL, Ghosh J. Novel use of arm ergometry cardiopulmonary exercise testing for non-elective patients with chronic limb-threatening ischaemia: a feasibility trial. BMJ Open. 2026 Jun 15;16(6):e118841. doi: 10.1136/bmjopen-2026-118841. PMID 42297459

Identifiers

NCT: NCT06404229 · 329960

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗