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NCT05711290 | Completed | Pulmonary Fibrosis


Oxygen Nanobubble Drink Impact on Exercise in Pulmonary Fibrosis
Sponsor:

University of Oxford

Brief Summary:

Approximately 1 in 5 (or 12.7 million adults) in the UK have longstanding respiratory illnesses, and 6.5 million patients report taking prescription medication to ease the burden. Many patients suffer from lung tissue damage, which impairs adequate blood oxygenation and reduces blood saturations, and causes breathlessness. The current method of treatment is palliative - with the patient breathing supplemental oxygen through an oxygen cylinder and tube. This severely compromises patients' quality of life, as they are tethered to a heavy, unwieldy oxygen cylinder, limiting their ability and willingness to leave home. Several recent studies in both animals and humans have indicated that orally administered oxygenated nanobubbles is a safe intervention that can improve tissue oxygenation. This randomized, double-blinded, cross-over, placebo-controlled study will evaluate the effect of an oxygen nanobubbles drink on the exercise performance of patients with chronic lung disease, such as pulmonary fibrosis. Patients will conduct the 6 Minute Walk Test (6MWT) twice, once with a placebo drink and once with the oxygen nanobubbles drink, based on a double-blind randomization protocol, and this study will evaluate the distance walked, heart rate, oxygen levels, breathlessness, and time to recovery in both cases. The investigators hypothesize that drinking the oxygen nanobubbles drink will improve the delivery of oxygen to vital organs, improving the distance a patient can cover in the 6 Minute Walk Test by 30m, which is the minimum clinically important difference.

Condition or disease

Pulmonary Fibrosis

Intervention/treatment

Oxygen Nanobubble

Placebo

Phase

Not Applicable

Study Type : Interventional
Estimated Enrollment : 28 participants
Masking : Triple
Primary Purpose : Treatment
Official Title : In Vivo Double-blind, Randomized, Placebo Controlled, Crossover Investigation of the Effect of Oral Administration of Oxygen Nanobubbles on the Distance Covered in a 6 Minute Walk Test in Patients With Pulmonary Fibrosis
Actual Study Start Date : March 21, 2023
Estimated Primary Completion Date : August 8, 2023
Estimated Study Completion Date : August 9, 2023
Arm Intervention/treatment

Experimental: Oxygen Nanobubble First

In this arm, the oxygen nanobubbles will be provided as a drink first. The oxygen nanobubbles mixture will be mixed with water and oxygenated. This will be provided as a one-time 200ml drink 10 minutes before the start of the 6 minute walk test. In this arm, the placebo will be provided as the second drink. This will be provided after atleast 2 hours after the first 6 minute walk test is completed. The placebo mixture will be mixed with water and oxygenated. This will be provided as a one-time 200ml drink 10 minutes before the start of the 6 minute walk test.

Dietary Supplement: Oxygen Nanobubble

Other: Placebo

Placebo Comparator: Placebo First

In this arm, the placebo will be provided as a drink first. The placebo mixture will be mixed with water and oxygenated. This will be provided as a one-time 200ml drink 10 minutes before the start of the 6 minute walk test. In this arm, the oxygen nanobubbles will be provided as the second drink. This will be provided after atleast 2 hours after the first 6 minute walk test is completed. The oxygen nanobubbles mixture will be mixed with water and oxygenated. This will be provided as a one-time 200ml drink 10 minutes before the start of the 6 minute walk test.

Dietary Supplement: Oxygen Nanobubble

Other: Placebo

Ages Eligible for Study: 18 Years
Sexes Eligible for Study: All
Accepts Healthy Volunteers: No
Criteria
Inclusion Criteria
  • Patient is Male or Female, aged 18 years or above
  • Participant is willing and able to give informed consent for participation in the study.
  • Patients diagnosed with Pulmonary Fibrosis as per ATS/ERS guidelines, and in whom the lung fibrosis is considered the dominant cause of symptoms (i.e. no severe other disease such as COPD or heart failure)
  • The patient must be able to walk independently without a walking stick
  • The patient can, in the view of their respiratory clinician, adequately participate in a 6MW test
Exclusion Criteria
  • Pregnant or breast feeding
  • History of current neurological condition (e.g., epilepsy)
  • Patient has consumed liquorice in the last 24 hours.
  • Patients with TLCO <30%
  • Patients with known unstable ischaemic heart disease or pulmonary hypertension
  • Patients with a history of smoking in the previous 30 days
  • Patients that are allergic or intolerant towards: Liquorice, Lecithin derived from soya or sunflower, Citric acid, Glycerol
  • Patients with known severe Renal Dysfunction
  • Patients with known severe Liver Dysfunction

Oxygen Nanobubble Drink Impact on Exercise in Pulmonary Fibrosis

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Oxygen Nanobubble Drink Impact on Exercise in Pulmonary Fibrosis

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Locations


Not yet recruiting

United Kingdom, Oxfordshire

Oxford University Hospitals NHS Foundation Trust

Oxford, Oxfordshire, United Kingdom, Cough solution

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