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OpenTrials
Active, Not Recruiting

NCT Number: NCT07428785

Pulmonary and Total Blood Volume in COPD

Background Patients with chronic obstructive lung disease (COPD) suffer from a progressive loss of lung function that leads to poor quality of life, and often invalidity and early death. This is markedly affected by a reduced exercise capacity and dyspnoea, but the underlying mechanisms are unknown. In the present study, we aim to investigate whether this may involve a reduced pulmonary blood volume secondarily to a reduced total blood volume.

Methods Design: Prospective matched comparative study Intervention: None

Outcomes:

The primary outcome is pulmonary blood volume estimated to total blood volume ratio between patients with COPD and healthy controls individually matched for age, sex, and height.

Statistical design:

All statistical analyses will be performed using R statistical software version 4.1.1 (R Project for Statistical Computing) within RStudio statistical software version 1.4.1717 (RStudio), and a two-tailed p<0.05 will be considered statistically significant. Inspection of normality and variance homogeneity will be done by creating qq-plots and histogram.

Regulatory considerations: This study will be submitted for approval by Regional Ethical Committee.

Perspective: This study will help uncover fundamental aspects of the pathophysiology of COPD.

Active, Not Recruiting

This study is active but is not currently recruiting participants.

Key information

About this study

Chronic obstructive pulmonary disease (COPD) is a leading cause of morbidity and mortality worldwide. Pulmonary rehabilitation is a cornerstone in the management of COPD and it is considered the most effective non-pharmacological intervention for improving quality of life. However, its wider use is limited by an incomplete understanding of the mechanisms underlying exercise-induced improvements in COPD. Exercise training is generally thought to exert little effect on lung function, at least when assessed by dynamic spirometry or diffusion capacity measured at rest in the upright position. Rehabilitation is mainly considered a mean to alleviate symptoms, primarily by improving skeletal muscle function, but without the potential to reverse any structural changes within the pulmonary system, which are seen in patients with COPD. The rationale for recommending exercise as a way to reduce symptom burden and increase quality of life, is based on the finding from the most recent Cochrane review.

An early feature of COPD is pulmonary vascular dysfunction, characterized by loss of pulmonary capillaries driven by a disease-specific imbalance between angiogenic and angiostatic processes. Indeed, this is likely a mechanism that drives the progressive loss of lung tissue, and also limits exercise capacity as the ability to expand the alveolar-capillary membrane though pulmonary capillary recruitment and distension becomes limited, thereby critically attenuating oxygen uptake during exercise. These pulmonary vascular abnormalities lead to a reduction in pulmonary blood volume (PBV), a phenomenon particularly evident in the supine position, where blood is mobilised from the lower extremities and abdomen to the pulmonary circulation, thus recruiting and distending the available pulmonary capillaries. Using 82Rb-PET, we recently demonstrated that PBV is markedly reduced in patients with COPD. However, it remains to be established whether this reduction reflects pulmonary vascular dysfunction or is simply secondary to systemic hypovolaemia, as total blood volume (TBV) has not yet been characterized in this population.

In the present study, we therefore aim to compare TBV and PBV in patients with COPD to those of age-, sex, and height-matched healthy controls.

Objectives:

Primary objective: To investigate whether patients with COPD exhibit systemic hypovolaemia.

Secondary objectives: To investigate whether the COPD-associated reduction in PBV is caused by a reduced TBV and the extent to which this limits exercise capacity.

Research hypotheses:

Primary: Patients with COPD exhibit a lower PBV/TBV-ratio than healthy individuals.

Secondary: Patients with COPD exhibit both a lower pulmonary capillary blood volume (VC), PBV, and TBV, exercise capacity, and rest-to-exercise increase in pulmonary diffusing capacity than healthy individuals.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Inclusion criteria -patients
  • Men and women
  • 45-80 years
  • COPD (GOLD stage I to III)
  • Resting arterial oxygenation > 90% Inclusion criteria - controls
  • Men and women
  • 45-80 years
  • Normal FEV1, FVC, FEV1/FVC, and single-breath diffusion capacity
  • Same sex, age (± 3 years) and height (± 5 cm) as an included COPD patient
  • Low- to moderate activity level defined as < 1,5 hours of structured physical activity pr. week at moderate intensity and cycling < 30 minutes/5km pr. day at moderate intensity (moderate intensity = out of breath but able to speak)

Exclusion criteria

Exclusion criteria

- patients

  • Symptoms of ischaemic heart disease
  • Known heart failure
  • Previous severe or current COVID-19
  • Claudication
  • Symptoms of disease within 2 weeks prior to the study
  • Participation in pulmonary rehabilitation within 6 months
  • Known malignant disease
  • Pregnancy
  • Unstable cardiac arrhythmic disease
  • Renal or liver dysfunction

Exclusion criteria

- controls

  • Known chronic lung disease
  • Known ischaemic heart disease
  • Known heart failure
  • Previous severe or current COVID-19
  • Symptoms of disease within 2 weeks prior to the study
  • Known malignant disease
  • Claudication
  • Pregnancy
  • Unstable cardiac arrhythmic disease
  • Renal or liver dysfunction

Treatment and study plan

Primary outcomes

  1. Between-group difference in Pulmonary- and total blood volume ratio (PBV/TBV-ratio)

    Time frame: day 2

Secondary outcomes

  1. pulmonary capillary blood volume/pulmonary blood volume ratio (VC/PBV-ratio)

    Time frame: day 2

  2. Between-group difference in total blood volume (TBV)

    Time frame: day 2

  3. Between-group difference in Pulmonary blood volume (PBV)

    Time frame: day 2

  4. Between-group difference in total red blood cell volume

    Time frame: day 2

  5. Between-group difference in total plasma volume

    Time frame: day 2

  6. Between-group difference in the pulmonary diffusing capacity to (nitric oxide) DL,NO (mmol/(min kPa)) at 60% of maximal workload

    Time frame: day 2

  7. Between-group difference in the pulmonary diffusing capacity to (nitric oxide) DL,NO (mmol/(min kPa)) at 50W

    Time frame: day 2

Other outcomes

  1. Between-group difference in lung tissue mass (LTM)

    Time frame: day 2

  2. Between-group difference in diffusion capacity, nitrogen oxide ( DL,NO) (mmol/(min kPa)) during upright rest

    Time frame: day 2

  3. Between-group difference in diffusion capacity, nitrogen oxide (DL,CO,5s) (mmol/(min kPa)) during upright rest

    Time frame: day 2

  4. Between-group difference in Pulmonary capillary blood volume (VC) during upright rest

    Time frame: day 2

  5. Between-group difference in alveolar-capillary membrane diffusing capacity (DM, mmol/(min kPa)) during upright rest

    Time frame: Day 2

  6. Between-group difference in cardiac output (L/min) during exercise at 60% of maximal workload.

    Time frame: day 2

  7. Between-group difference in relative (mL/kg/min)

    Time frame: day 1

  8. Between-group difference in body composition: total mass (kg)

    Time frame: Day 1

  9. Between-group difference: Forced expiratory volume 1 second (FEV1 (L and %pred))

    Time frame: day 1

  10. Between-group difference in mean bolus transit time (s) (supine rest)

    Time frame: day 2

  11. Between-group difference in mean bolus transit time (s) (adenosine infusion)

    Time frame: Day 2

  12. Between-group difference in global coronary flow reserve (mL/min)

    Time frame: day 2

  13. Between group difference in pulmonary blood volume reserve (mL)

    Time frame: day 2

  14. Between-group difference in left ventricular ejection fraction (%)

    Time frame: day 2

  15. Between-group difference in coronary calcium score

    Time frame: day 2

  16. Between-group difference in resistance (Rrs, R5-R20) measured by IOS

    Time frame: day 1

  17. Between-group difference in reactance (Xrs, X5) measured by IOS

    Time frame: day 1

  18. Between-group difference in daily physical activity level measured by AX3 (steps and intensity)

    Time frame: day 2

  19. Between-group difference in absolute (mL/min) V̇O2peak

    Time frame: Day 1

  20. Between-group difference in ventilatory threshold (%)

    Time frame: Day 1

  21. Between-group difference in ventilatory reserve (%)

    Time frame: Day 1

  22. Between-group difference in body composition: total fat mass (kg and %)

    Time frame: Day 1

  23. Between-group difference in body composition: lean body mass (kg)

    Time frame: Day 1

  24. Between-group difference in body composition: fat percentage (%)

    Time frame: day 1

  25. Between-group difference: Forced vital capacity (FVC (L and %pred))

    Time frame: Day 1

  26. Between-group difference: Residual capacity (RV (L and %pred))

    Time frame: day 1

  27. Between-group difference: Total lung capacity (TLC (L and %pred))

    Time frame: Day 1

  28. Between-group difference: single-breath diffusion capacity to carbon monoxide (mmol/(min kPa) and %pred)

    Time frame: day 1

Sponsors and collaborators

Lead sponsor

Rigshospitalet, Denmark

Other

Registry information

Official study title

Pulmonary and Total Blood Volume in COPD: A Prosoective Matched Comparative Study

Acronym: COPD-TBV

Important dates

Study start
2025
Primary completion
2026
Study completion
2026
First posted
Feb 24, 2026
Registry last updated
Feb 24, 2026

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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