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Beetroot juice may boost exercise in lung scarring disease

NCT ID NCT06488638

What the study statuses mean

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Recruitment status, easiest to join first

Recruiting now This study
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

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

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

About 16 people

The number the study aims to enrol. It can still change while the study runs.

Started

Feb 2026

Expected to finish

Jun 2027

An estimate. End dates often move.

Lead sponsor

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

18 to 85 years

Sex

Anyone

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

Show the full entry requirements

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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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

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How to take part

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  1. The study's own enquiry address

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  2. The places running it

    1 site. The list below names each one and where it is.

  3. The official record

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    Open the record ↗

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Contacts and locations

Locations

  • University Hospital Southampton

    RECRUITING

    Southampton, SO16 6YD, United Kingdom

    Contact Email: •••••@•••••

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