Actively Recruiting

Age: 18Years +
All Genders
Healthy Volunteers
NCT06465277

CMR Right Ventricular Contractile Reserve Following Lung Resection

Led by Belfast Health and Social Care Trust · Updated on 2024-10-03

42

Participants Needed

1

Research Sites

71 weeks

Total Duration

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AI-Summary

What this Trial Is About

Feasibility study investigating CMR dobutamine stress testing before and after lung resection

CONDITIONS

Official Title

CMR Right Ventricular Contractile Reserve Following Lung Resection

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Provision of informed consent
  • Age over 16 years
  • Planned elective lobectomy lung resection, oesophagectomy with one lung ventilation, or gastrectomy surgery
Not Eligible

You will not qualify if you...

  • Pregnancy
  • Ongoing participation in any investigational research that could affect this study
  • Atrial fibrillation at baseline
  • Contraindications to CMR including cardiac pacemaker, artificial heart valve, neurostimulator, cochlear implant, aneurysm clips, metal injuries to the eye, or loose metal in the body
  • Contraindications to dobutamine stress testing such as severe systemic arterial hypertension (≥220/120 mmHg), unstable angina, severe aortic valve stenosis (peak gradient >60mmHg or valve area <1cm2), complex cardiac arrhythmias including uncontrolled atrial fibrillation, hypertrophic obstructive cardiomyopathy, myocarditis, endocarditis, pericarditis, or uncontrolled heart failure
  • Lung resection specific exclusions including wedge, segmental or sub-lobar lung resection, pneumonectomy, or isolated right middle lobectomy

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Belfast Health and Social Care Trust

Belfast, Northern Ireland, United Kingdom, BT12 6BA

Actively Recruiting

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Research Team

A

Adam Glass

CONTACT

J

Jon Silversides

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

3

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