Beetroot juice may boost exercise in lung scarring disease
NCT ID NCT06488638
First seen Jun 30, 2026 · Last updated Jul 07, 2026 · Updated 3 times
Summary
This study investigates whether drinking nitrate-rich beetroot juice twice a day for three days can improve exercise capacity in people with idiopathic pulmonary fibrosis (IPF), a lung scarring disease that limits activity. Researchers will compare the juice to a placebo in a small group of 8 IPF patients and also measure blood markers and blood flow. The goal is to see if this simple supplement can help patients exercise longer.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- nitrate-rich beetroot juice
- What this could lead to
- If it works, this could point toward a simple dietary supplement to help IPF patients exercise more easily.
- What could go wrong
- This is a very small pilot study with only 8 IPF patients, so results may not apply broadly. The supplement may show no benefit or cause side effects like stomach upset.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 16 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Feb 2026
- Expected to finish
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Jun 2027
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 85 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
IPF Patients: Inclusion Criteria 1. Patients aged 18-85 years with a prior specialist multidisciplinary team diagnosis of idiopathic pulmonary fibrosis (IPF) based on current established consensus guidelines. 2. Medical Research Council (MRC) breathlessness grade 1-3 3. Judged clinically stable for 3 months prior to recruitment by the investigator. IPF Patients: Exclusion Criteria 1. Baseline spirometry with FEV1/FVC ratio \< 0.7. 2. Neoplastic disease undergoing treatment or active follow up. 3. Presence of infection or exacerbation requiring hospitalization, within last 3 months. 4. Current tobacco smoker or use of nicotine containing vapes (within 3 months) 5. Current use of ambulatory or long-term oxygen therapy (LTOT). 6. Peripheral oxygen saturations \<85% during 6-minute walk-test. 7. Any condition which would prevent completion of cycle-ergometer testing, pulmonary function testing (PFT) or 6-minute walk testing as judged by the investigator. 8. Participation in a pulmonary rehabilitation (PR) program in the last 3 months. 9. Any condition excluding CPET based on the absolute contraindication as the ACCP/ATS guidelines 2003 10. Positive pregnancy test in females of childbearing age. 11. Symptomatic peripheral vascular disease 12. Concomitant use of nitrate-based medicine or phosphodiesterase V inhibitors Controls: Inclusion Criteria 1\) Age and sex-matched to participants in the IPF cohort. Note: the participants will be age-matched within a 5-year age bracket. Controls: Exclusion Criteria 1. Inability to give informed written consent. 2. Malignancy (except localised squamous or basal cell skin carcinoma) undergoing active investigation, treatment, or follow-up. 3. Significant cardiorespiratory disease as judged by the investigator. 4. Diabetes mellitus requiring treatment with pharmacology therapy. 5. Current tobacco smoker or use of nicotine containing vapes (within three months). 6. Symptomatic peripheral vascular disease. 7. Concomitant use of nitrate-based medicine or phosphodiesterase V inhibitors.
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Genom att skicka in godkänner du våra Användarvillkor
Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The study's own enquiry address
This study publishes an address for enquiries. See it below .
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
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Contacts and locations
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Genom att skicka in godkänner du våra Användarvillkor
Locations
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University Hospital Southampton
RECRUITINGSouthampton, SO16 6YD, United Kingdom
Contact Email: •••••@•••••
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