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NCT Number: NCT02949531

Use of Oxygen in Heart Failure With Preserved Ejection Fraction

Oxygen is routinely given to patients with common conditions such as COPD and heart failure. There is no evidence behind giving oxygen to patients specifically in heart failure due to a stiff heart.

This study aims to explore the effect oxygen has on the ability of patients with chronic heart failure and the ability to exercise. Other common variables will be assessed such as heart rate and blood pressure to observe the response to varying concentrations of oxygen.

The concentrations chosen are commonly offered in hospitals and indeed are being delivered through standard equipment found in all hospitals in the country.

It is hoped that studying the effect of short term oxygen on patients with heart failure will help to identify the effectiveness of oxygen in longer term therapy for patients who are often breathless with a decreased exercise tolerance.

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Key information

Age range

50 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

About this study

Many patients with reduced exercise tolerance have a preserved left ventricular function. These patients are labelled as having heart failure with preserved ejection fraction (HeFPEF), when the combined use of echocardiography and biochemistry. The prevalence and the incidence of HeFPEF are on the increase and currently it accounts for around 50% of all patients diagnosed with HF. The last twenty years of research has led to great improvement in available treatments for heart failure with reduced ejection fraction (HeFREF); however, current guidelines only suggest diuretics to improve symptoms of those patients with HeFPEF: clinical trials of several pharmacological interventions have failed to show convincing reductions in morbidity or mortality for patients with HeFPEF.

The effect of oxygen therapy on exercise capacity has remained poorly understood in HeFREF and, at the time of writing this study, it has never been explored in HeFPEF. The investigators recently completed a study showing an increase in exercise time, exercise load at peak exercise and peak metabolic equivalent on cycle ergometry with 28% oxygen supplementation and further increments when 40% oxygen supplementation was used in patients with heart failure with reduced ejection fraction.

The investigators aim to improve exercise time in patients with HeFPEF with oxygen supplementation. Identifying the correct dose of oxygen will be a further aim to avoid hyperoxygenation but provide adequate oxygen to improve exercise tolerance.

Patients will be identified from heart failure clinics and will be invited for screening visit. Eligible patients will have three treatment visit at least one week apart (each visit with a different oxygen concentration i.e room air, 28% and 40% oxygen, randomly determined by sealed envelopes)

Patients will use standard cycle ergometry to exercise and work load will be increased every minute by 5-10 watts. Patients will be encouraged to cycle until tired. At the end of cycling, exercise time, peak metabolic equivalent, work load, shortness of breath score will be noted at each visit.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Over 50 years of age and able and willing to give consent
  • Have signs and/or symptoms of heart failure
  • Left ventricular ejection fraction > 45%
  • NT-pro BNP > 220 pg/ml (in the previous 12 months)
  • On any diuretic

Exclusion criteria

  • Unable or unwilling to give consent
  • Recent (<1 month) acute myocardial infarct or cerebrovascular event
  • Significant renal dysfunction (eGFR <30 ml.min-1.1.73m-2)
  • Significant anaemia (Haemoglobin < 100 g.L-1)
  • Systolic blood pressure <90 mmHg, or >180 mmHg
  • Severe mitral or aortic valve disease
  • Diagnosis of severe chronic lung disease
  • Involvement in another medicinal trial within the past four weeks
  • Unable to use cycle
  • Any planned admission in the following 3-4 weeks (patient can be reconsidered for enrolment after planned admission)

Treatment and study plan

Oxygen

Drug

Primary outcomes

  1. change in exercise time with the use of 21%, 28% and 40% oxygen

    Time frame: at 3 weeks

    the total time cycled in each arm

Secondary outcomes

  1. change in shortness of breath with the use of 21%, 28% and 40% oxygen

    Time frame: at 3 weeks

    shortness of breath measured using BORG score

  2. change in Peak metabolic equivalent with the use of 21%, 28% and 40% oxygen

    Time frame: at 3 weeks

    measured using standard peak metabolic equivalent

Sponsors and collaborators

Lead sponsor

Hull University Teaching Hospitals NHS Trust

Other Gov

Registry information

Official study title

Randomised, Cross Over, Single Blind, Control Trial of Short Term Oxygen Use During Cycle Ergometry in Patients With Chronic Heart Failure With Preserved Ejection Fraction

Acronym: STOP-EF

Important dates

Study start
2016
Primary completion
2017
Study completion
2017
First posted
Oct 31, 2016
Registry last updated
Jun 26, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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