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Assessing the Accuracy of Seismofit® as an Estimate of VO2 Peak in Patients With Hepato-pancreato-biliary, Colorectal, and Gastro-oesophageal Cancer (VERVE)

R

Royal Marsden NHS Foundation Trust

Status

Enrolling

Conditions

Oesophageal Cancer
Gastric Cancer
Hepato-Biliary Carcinoma in Situ Nos
Colorectal Cancer
Pancreatic Cancer

Treatments

Other: Non-Interventional

Study type

Observational

Funder types

Other

Identifiers

NCT05831488
CCR5651

Details and patient eligibility

About

Our study aims to assess the relationship between the Seismofit® derived VO2 peak estimate and CPET-measured VO2 peak in patients who are having CPET as part of their preoperative workup. Our aim is to establish whether Seismofit® can be considered a cheaper, less resource intensive and better tolerated alternative to the CPET, or whether it might be useful as a screening tool to efficiently identify patients with exercise intolerance who may benefit from further characterisation by CPET.

Enrollment

35 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Age ≥18
  2. Scheduled for elective surgery for resection of HPB, colorectal or gastro-oesophageal primary or secondary cancer
  3. Undergoing CPET as part of routine pre-operative investigations

Exclusion criteria

  1. Subjects unable to give voluntary written informed consent to participate in this study
  2. Diagnosis of moderate or worse stenosis or regurgitation of any cardiac valve
  3. Previous aortic or mitral valve surgery, valvuloplasty or transcatheter valve implantation
  4. Permanent pacemaker or cardiac resynchronisation device in situ
  5. Diagnosis of severe pulmonary hypertension
  6. Permanent atrial fibrillation

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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