Oxygen Nanobubble Drink Impact on Exercise in Elite Athletes

Healthy Clinical Trial

Official title:

in Vivo Double-blind, Randomized, Placebo Controlled, Crossover Investigation of the Effect of Oral Administration of an Oxygen-nanobubble Drink on the Exercise Performance in Elite Athletes

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT05777642
• Other study ID #: R83003/RE001
• Status: Not yet recruiting
• Phase: N/A
• Start date: April 20, 2023
• Est. completion date: June 18, 2024

Study information

• Verified date: February 2023
• Source: University of Oxford
• Contact: Mihir Sheth
• Phone: 01865617683
• Email: mihir.sheth[@]nds.ox.ac.uk
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Although the primary organ of gas exchange is the lung, it has been recognized for some time that other organs have a potential role in gas exchange. There is emerging evidence that the gastrointestinal tract may have the capacity to act as an organ of gas exchange. Several recent studies in both animals and humans have indicated that orally administered oxygenated nanobubbles is a safe intervention that can improve tissue oxygenation. Oxygen nanobubbles can reduce the hypoxia in tumours when injected, in conjunction with sonodynamic therapy. In mice, researchers have shown a reduction in tumour hypoxia and improved response to sonodynamic therapy occurs even when the oxygen nanobubbles are orally administered. This will be an in vivo randomized, double-blinded, cross-over, placebo-controlled study consisting of rowers. By measuring the time taken by participants to complete a 2000m row after consuming an Oxygen nanobubbles drink, and a placebo drink, the investigators will evaluate the efficacy of the nanobubbles on the exercising ability of the participant.

Description:

Although the primary organ of gas exchange is the lung, it has been recognized for some time that other organs have a potential role in gas exchange. There is emerging evidence that the gastrointestinal tract may have the capacity to act as an organ of gas exchange. Several animal studies have demonstrated that oxygen (delivered as a gas and within enriched water) is capable of diffusing through the mucosa of the colon, peritoneum and stomach resulting in elevated oxygen tension in the splanchnic circulation (hepatic portal vein, arterial and venous mixed blood) and increased blood flow (portal venous blood flow). One MRI study has demonstrated that orally administered oxygen-supersaturated water causes a significant increase in the luminal oxygen concentration in both the oral cavity and the stomach, despite a low amount of oxygen added to the overall oxygen balance of the body. Several recent studies in both animals and humans have indicated that orally administered oxygenated nanobubbles is a safe intervention that can improve tissue oxygenation. Oxygen nanobubbles can reduce the hypoxia in tumours when injected, in conjunction with sonodynamic therapy. In mice, researchers have shown a reduction in tumour hypoxia and improved response to sonodynamic therapy occurs even when the oxygen nanobubbles are orally administered. A study of male cyclists also showed that ingested oxygen nanobubbles led to an increased power output. This will be an in vivo randomized, double-blinded, cross-over, placebo-controlled study consisting of rowers. By measuring the time taken by participants to complete a 2000m row after consuming an Oxygen nanobubbles drink, and a placebo drink, the efficacy of the nanobubbles on the exercising ability of the participant will be evaluated. This will be supplemented with a comparison of a pre-intervention and post-intervention validated Rate of Perceived Exertion (RPE) breathlessness questionnaire and measurement of blood lactate and glucose, blood gases, respiratory gas exchange and heart rate.

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 42
• Est. completion date: June 18, 2024
• Est. primary completion date: May 18, 2024
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Participant is willing and able to give informed consent for participation in the research
• Participant is 18+ years of age
• Not currently taking any medications (except the contraceptive pill)
• The participant must be a competitive rower, with an estimated 2000m time of =6:30 minutes for males, and = 8 minutes for females.
• The participant agrees to abstain from tobacco and nicotine products 24 hours before each visit.
• The participant agrees to abstain from alcohol 24 hours before each visit.
• The participant is, in the opinion of the investigator, healthy on the basis of a self-reported medical history, vital signs.
• The participant has no active disease process that could interfere with endpoints.
• Available for the duration of the study.
• The participant is not taking regular medications (including NSAIDs such as ibuprofen) that could interfere with endpoints measured and/or influence gastrointestinal permeability and led to gastrointestinal symptoms.
• The participant has not taken dietary/nutritional supplements in the preceding 2 weeks.
• The participant is not following a weight reducing diet.
• The participant is willing not to undertake strenuous or unaccustomed physical exercise for at least 24 hours prior to screening and study visits.

Exclusion Criteria:

• Participants with a history of smoking in the previous 30 days
• Participants that are allergic or intolerant towards: Liquorice, Lecithin derived from soya or sunflower, Citric acid, Glycerol
• Clinically significant cardiovascular, respiratory, hepatic, renal, gastrointestinal, endocrine, neurological, immunological, or haematological disease or abnormality, as determined by the self-reported health questionnaire.
• History of alcohol, narcotic, benzodiazepine, or other substance abuse or dependence within the 12 months preceding study visit 1.
• Currently participating in another study with an investigational or non-investigational drug or device, or has participated in another clinical study within the 2 months preceding study visit 1 (based on participant's self report).
• Any condition that, in the investigator's opinion, compromises the participant's ability to meet protocol requirements or to complete the study.
• Participant is pregnant and/or breastfeeding

Related Conditions & MeSH terms

• Healthy

Intervention

Dietary Supplement:
• Oxygen Nanobubble
This contains oxygenated nanobubbles made from lecithin and natural flavourings (Liquorice, glycerol, and citric acid)
• Placebo
This does not contain nanobubbles and is made from natural flavourings (Liquorice, glycerol, and citric acid)

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
University of Oxford

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	2000m Row Time	Time taken to complete 2000m Row	7 days
Secondary	Heart Rate	Changes in the Heartrate before and after the 2000m Row with the oxygen nanobubbles drink compared with the placebo drink	7 days
Secondary	Peripheral Oxygen Saturation (SpO2)	Changes in the Oxygen Saturation (SpO2) before and after the 2000m Row with the oxygen nanobubbles drink compared with the placebo drink.; The oxygen saturation (SpO2) will be measured by a pulse oximeter on a scale of 0-100%.	7 days
Secondary	Rate of Perceived Exertion	Changes in the Rate of Perceived Exertion before and after the 2000m Row with the oxygen nanobubbles drink compared with the placebo drink.; This uses the Borg scale from 6-20, where 6 indicates light exertion, and 20 indicates maximal exertion	7 days
Secondary	Blood Lactate	Changes in the blood lactate before and after the 2000m Row with the oxygen nanobubbles drink compared with the placebo drink.	7 days
Secondary	Blood Glucose	Changes in the blood glucose before and after the 2000m Row with the oxygen nanobubbles drink compared with the placebo drink.	7 days