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Testing a helium-oxygen gas mix for breathlessness in heart failure with obesity

Tests a helium-oxygen gas mix during exercise in adults with heart failure and obesity.

Plain-language title generated from the registry record
Registry title: Targeting Breathing Limitations to Improve Functional Outcomes in HFpEF

Key facts

Where
Dallas, United StatesSee the site

AI summary: who the study is looking for

From the trial's eligibility criteria. Machine-read from the registry text on this page, so it can be wrong. The registry text below and the trial team decide who can take part.

The trial is looking for adults aged 55 to 90 with heart failure with preserved ejection fraction (HFpEF) and obesity. It studies whether breathing limits cause breathlessness and low exercise capacity.

Age
55 to 90 years
Sex
All sexes can join.
Disease stage
Signs and symptoms of heart failure, ejection fraction above 0.50, and signs of diastolic dysfunction (raised NT-proBNP above 300 ng/dl or a hospital stay for heart failure).
Earlier treatment
People using a phosphodiesterase type 5 (PDE5) inhibitor cannot join.
Biomarker or test result
Raised NT-proBNP above 300 ng/dl, or a hospital stay for heart failure.

Main reasons for not taking part

  • Age under 55 years
  • BMI above 50 kg/m2
  • Atrial fibrillation with poorly controlled heart rate
  • Severe valve disease
  • Severe chronic obstructive pulmonary disease (COPD)

Read by machine on 9 November 2026.

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 55 and 90 years old?

Source: NCT05723679, who can take part

Where in United States

  • UT Southwestern Medical CenterDallas, United StatesContact: Raksa B Moran, RNTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?

Contact the study team: see the registry record → Contacts and Locations

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Trial details

Who runs it
University of Texas Southwestern Medical Center
Trial code
NCT05723679
Record updated
7 May 2026
Original description
The overall purpose of this study is to investigate whether pulmonary limitations that increase the oxygen (O2) cost of breathing impact dyspnea on exertion (DOE) and peak exercise capacity in patients with HFpEF and obesity. As per investigator's hypothesis, obesity is likely a significant contributor to DOE and exercise intolerance in patients with HFpEF.Read full original descriptionShow less

Targeting Breathing Limitations to Improve Functional Outcomes in Heart Failure With Preserved Ejection Fraction (HFpEF)

The overall purpose of this study is to investigate whether pulmonary limitations that increase the oxygen (O2) cost of breathing impact dyspnea on exertion (DOE) and peak exercise capacity in patients with HFpEF and obesity. As per investigator's hypothesis, obesity is likely a significant contributor to DOE and exercise intolerance in patients with HFpEF.

Inclusion: signs and symptoms of heart failure; an ejection fraction > 0.50; objective evidence of diastolic dysfunction. elevated biomarkers (NT-proBNP >300 ng/dl) or HF hospitalization; healthy volunteers.

Exclusion: phosphodiesterase type 5 (PDE5) inhibitor use; Atrial fibrillation with poorly controlled heart rate; severe valvular disease; severe Chronic obstructive pulmonary disease (COPD); Chronic kidney disease (CKD) 4 or higher; age < 55 years; BMI > 50 kg/m2; any restriction of ambulation and mobility.

ClinicalTrials.gov NCT05723679