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NCT Number: NCT06758531

Coffee Bioequivalence Trial

The goal of this clinical trial is to test if coffee consumed as a tablet is biologically equivalent to that consumed traditionally as a drink. It will also learn about the impact of the short-term intake of coffee on markers of cardiovascular and liver health. The main questions it aims to answer are:

* Do coffee bioactive compounds produce the same levels in blood and urine regardless of how the coffee is consumed (tablet or drink)? * How does coffee as a tablet or drink impact cardiovascular risk and liver health versus a non-coffee control?

Participants will:

* Visit the clinical unit for three phases; each phase is 1x 480 minute (eight hour) acute postprandial visit and 1 x one hour visit the following day. During each phase they will be randomly assigned to take a different intervention (coffee drink, coffee tablet, coffee-free control) * Be cannulated during the 480 minute (8 hour) acute visits and have regular blood draws as well as basic clinical assessments * Return on day two for a fasting blood sample and basic clinical assessment * Collect their urine for 24 h * Be asked to record their intake of foods and drinks for 3 days to assess their usual diet (dietary assessment).

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Key information

Age range

18 year–45 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Hugh Sinclair Unit of Human Nutrition, Department of Food and Nutritional Sciences, University of Reading

Reading, Berkshire, RG6 6DZ, United Kingdom

Location contact

Altaf Farraj, MSc

CONTACT

Anisha Wijeyesekera, PhD

CONTACT

Charlotte E Mills, PhD

CONTACT

Hugh Sinclair Manager

CONTACT

[email protected]

0118378 ext. 7771

Kim G Jackson, PhD

CONTACT

Lolwa Alawadhi, MSc

CONTACT

Tijesu Akeredolu

CONTACT

About this study

Coffee has gained interest for its role in the prevention of non-communicable diseases such as heart and liver diseases. Population-based studies have reported that consuming 2-4 cups of coffee per day is associated with lower death rates and, notably reductions in the incidence of heart disease. However, these observational trials do not directly prove causality and carefully designed randomised controlled trials are needed.

This current trial will provide vital information to inform a large-scale randomised controlled trial assessing the effects of coffee consumption on risk markers for developing cardiometabolic disease (such as type 2 diabetes, heart and liver diseases) to test causality. In this follow-up trial to be conducted in 2025, non-coffee consumers will be recruited. To maximise recruitment, retention and adherence in the trial, we are considering providing instant coffee as tablets rather than as a drink. Hence, the current study will help to understand if coffee delivered in a tablet is biologically equivalent to consuming coffee as a drink.

A 3 armed, randomised, controlled crossover trial in healthy participants wil be performed. The primary outcome is the pharmacokinetic profile of coffee bioactives in coffee drink versus the coffee tablet. Secondary outcomes will be assessing the impact of the coffee both as a drink and tablet on cardiovascular and liver health markers (versus a coffee-free control).

Briefly, participants will attend three study phases. Each study phase includes a 480 minute (8-hour) acute postprandial visit and a shorter visit (~one hour) the following morning. On the first day participants will arrive having fasted overnight and having followed dietary and lifestyle restrictions in the preceding days. They will have baseline anthropometric measures performed and a cannula will be inserted; two baseline blood samples will be collected (14 mL in total). Blood samples will be collected regularly from the cannula, and a clinic blood pressure measurement will be performed at regular intervals following the intervention (a different intervention will be given in a random order at each of the three phases). A breakfast meal and lunch will be provided to the participants during the visit and participants will leave with a standardised meal and snack to consume in the evening. They will return, fasted the following morning to provide a blood samples and have their blood pressure measured. Participants will be asked to collect their urine for 24h following the intervention; this will be returned that morning. There will be a 4-week period between each study phase.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Healthy males and pre-menopausal females (must have regular menstrual cycles)
  • Aged between 18 to 45 years
  • Body mass index (BMI) between 18.5-30 kg/m2

Exclusion criteria

  • Sensitivity to coffee and caffeine
  • Food allergies relating to the test meals provided (such as gluten or lactose intolerance)
  • Current smoking and vaping use.
  • Medical history of chronic diseases (cancer, high blood pressure (hypertension), type 2 diabetes, heart attack and/or any other heart disease related diseases, gastrointestinal disorders, hyperlipidaemia, kidney or liver disease).
  • Diagnosed with anaemia
  • Prescribed any medication relating to the study outcome measures (such as blood pressure lowering, anti-inflammatories or blood thinners).
  • Drinking more than the recommended intake for alcohol (> 14 units/week)
  • Taking any supplements (vitamins, minerals, probiotics).
  • Any other unusual medical history or diet and lifestyle habits or practices that would preclude volunteers from participating in a dietary intervention and metabolic study (e.g. pacemaker)
  • Planning on a weight-reducing regimen (lost >3 kg in the last 6 months)
  • Parallel participation in another intervention study
  • Pregnancy, planning a pregnancy in the next 6 months or breastfeeding
  • NHS blood donation in the last 3 months

Treatment and study plan

Instant coffee given as a drink

Dietary Supplement

Commercially available instant coffee (3.6 g) will be provided in the form of a drink prepared with 400 ml of water. A standard breakfast consisting of cereal with milk will be provided at 60 mins after the intervention. A standard lunch (cheese sandwiches, potato crisps and shortbread biscuits) will be given at 300 after coffee intake.

Coffee given in a tablet form

Dietary Supplement

Commercially available instant coffee (3.6 g) will be provided as 4 tablets given with 400 ml of water. A standard breakfast consisting of cereal with milk will be provided at 60 mins after the intervention. A standard lunch (cheese sandwiches, potato crisps and shortbread biscuits) will be given at 300 after coffee intake.

Control (placebo)

Dietary Supplement

A caffeine and coffee free control (3.6 g) will be provided as 4 tablets given with 400 ml of water. A standard breakfast consisting of cereal with milk will be provided at 60 mins after the intervention. A standard lunch (cheese sandwiches, potato crisps and shortbread biscuits) will be given at 300 after coffee intake.

Primary outcomes

  1. Pharmacokinetic profile of key coffee biologically active compounds and their metabolites after consuming a coffee drink, a coffee tablet and control.

    Time frame: Blood taken prior to consuming the intervention (0 minutes) and then 30, 45, 60, 90, 120, 180, 240, 300, 360, 420, 480 and 1440 minutes post intervention.

    Key coffee biologically active compounds and their metabolites (e.g. chlorogenic acids, caffeine, trigonelline) will be measured in plasma samples collected over a 24 h period after each intervention. The pharmacokinetic profile (absorption, metabolism and excretion), maximal concentration, Cmax will be calculated.

  2. Pharmacokinetic profile of key coffee biologically active compounds and their metabolites after consuming a coffee drink, a coffee tablet and control.

    Time frame: Blood taken prior to consuming the intervention (0 minutes) and then 30, 45, 60, 90, 120, 180, 240, 300, 360, 420, 480 and 1440 minutes post intervention.

    Key coffee biologically active compounds and their metabolites (e.g. chlorogenic acids, caffeine, trigonelline) will be measured in plasma samples collected over a 24 h period after each intervention. The pharmacokinetic profile (absorption, metabolism and excretion), area under the concentration curve will be calculated.

Secondary outcomes

  1. Fasting concentrations of total cholesterol and high-density lipoprotein cholesterol.

    Time frame: Acute study days prior to the intervention (0 minutes).

    Serum lipids will be measured directly using a clinical chemistry analyser.

  2. Fasting and postprandial lipids concentrations after consuming the coffee drink, coffee tablet and control interventions

    Time frame: Acute study days, blood taken prior to the intervention (0 minutes) and then 15, 30, 45, 60, 90, 120, 180, 240, 300, 360, 420 and 480 minutes.

    Serum triacylglycerol and non-esterified fatty acids will be measured in the fasting and postprandial blood samples collected for 480 min after each intervention.

  3. Fasting and postprandial glucose concentrations after consuming the coffee drink, coffee tablet and control interventions

    Time frame: Acute study days, blood taken prior to consuming the intervention (0 minutes) and then 15, 30, 45, 60, 90, 120, 180, 240, 300, 360, 420 and 480 minutes.

    Serum glucose will be measured in the acute study day blood samples collected for 480 minutes after each intervention using a clinical chemistry analyser.

  4. Fasting and postprandial insulin concentrations after consuming the coffee drink, coffee tablet and control interventions

    Time frame: Acute study days, blood taken prior to consuming the intervention (0 minutes) and then 15, 30, 45, 60, 90, 120, 180, 240, 300, 360, 420 and 480 minutes.

    Serum insulin will be measured in the acute study day blood samples collected for 480 minutes after each intervention using an enzyme-lined immunosorbent assay.

  5. Fasting and postprandial liver enzyme concentrations after consuming the coffee drink, coffee tablet and control interventions

    Time frame: Acute study days, blood taken prior to consuming the intervention (0 minutes) and then 15, 30, 45, 60, 90, 120, 180, 240, 300, 360, 420 and 480 minutes.

    Serum alanine transaminase (ALT), aspartate transferase (AST), alkaline phosphatase (ALP), gamma-glutamyl transferase (GGT) and glutamate dehydrogenase (GLDH) will be measured in the acute study day blood samples collected for 480 minutes after each intervention using a clinical chemistry analyser.

  6. Fasting and postprandial gut hormone concentrations after consuming the coffee drink, coffee tablet and control interventions

    Time frame: Acute study days, blood taken prior to the intervention (0 minutes) and then 30, 60, 120, 180, 240, 300, 360 and 480 minutes.

    C-peptide, GIP, GLP-1 and Ghrelin will be measured in the postprandial blood samples collected for 480 min after each interventions.

  7. Fasting and postprandial plasma metabolomics after consuming the coffee drink, coffee tablet and control interventions

    Time frame: Acute study days, blood taken prior to the intervention (0 minutes) and then 30, 60, 120, 180, 240, 300, 360, 420 and 480 minutes.

    Metabolomics will be measured in the postprandial blood samples collected for 480 min after the interventions using NMR.

  8. Fasting and postprandial plasma nitrate and nitrite concentrations after consuming the coffee drink, coffee tablet and control interventions

    Time frame: Acute study days, blood taken prior to the intervention (0 minutes) and then 15, 30, 45, 60, 120, 180, 240, 300, 360, 420 and 480 minutes.

    Nitrate, nitrite and Nox (sum of nitrate and nitrite) will be measured in the postprandial blood samples collected for 480 min after each intervention.

  9. Urinary metabolomics

    Time frame: Urine will be collected prior to (0 minutes) and for 1440 minutes after each intervention.

    Metabolomics will be performed on the 24 h urine samples using NMR .

  10. Urinary creatinine

    Time frame: Urine will be collected prior to (0 minutes) and for 1440 minutes after each intervention.

    Creatinine will be measured in the 24 h urine samples using a clinical chemistry analyser.

  11. Urinary osmolality and pH

    Time frame: Urine will be collected prior to (0 minutes) and for 1440 minutes after each intervention.

    Osmolality will be determined as a measure of the concentration of solutes in the 24 h urine sample and pH to indicate whether the sample is acidic or alkaline after consuming the study interventions.

  12. Urinary sodium and potassium

    Time frame: Urine will be collected prior to (0 minutes) and for 1440 minutes after each intervention.

    Sodium and potassium will be determined in the 24 h urine sample as a marker of kidney function and a nutritional biomarker after consuming the study interventions.

  13. Body weight

    Time frame: On each acute study visit prior to the collection of the first blood sample (0 minutes).

    Body weight will be measured using a Tanita scale.

  14. Height

    Time frame: First acute study visit (0 minutes on visit 1)

    Height will be measured to the nearest cm using a stadiometer

  15. Blood pressure

    Time frame: -15, 30, 60, 120, 180, 240, 300, 360, 420, 480 minutes

    Blood pressure will be measured using blood pressure monitor.

  16. Body fat percentage

    Time frame: Each acute study visit (0 minutes)

    Body fat percentage will be measured using the Tanita scale by bioelectrical impedance.

  17. Body fat mass

    Time frame: On each acute study visit prior to the collection of the first blood sample (0 minutes).

    Body fat mass will be measured using a Tanita scale.

  18. Body lean mass

    Time frame: On each acute study visit prior to the collection of the first blood sample (0 minutes).

    Body lean mass will be measured using a Tanita scale.

  19. Body mass index

    Time frame: On each acute study visit (0 minutes)

    Body mass index will be calculated using the body weight (kg) and height (m) data.

  20. Waist and hip circumferences

    Time frame: On each acute study visit (0 minutes).

    A non-stretch tape will be used to measure waist and hip circumferences

  21. Habitual dietary intake of the study participants

    Time frame: Two weeks prior to the first acute study visit (t- 2 weeks from visit 1).

    Record of the food and drink prior to the first study visit

  22. Fasting estimate of insulin resistance and insulin sensitivity

    Time frame: On each acute study visit (0 minutes).

    HOMA-IR (Homeostasis model assessment estimated insulin resistance) and QUICKI (Quantitative Insulin Sensitivity Check Index) will be calculated using the fasting glucose and insulin data.

  23. Fasting low-density lipoprotein-cholesterol concentration

    Time frame: On each acute study visit (0 minutes).

    The low-density lipoprotein-cholesterol concentration will be calculated from aforementioned outcomes using the Friedewald formula.

Study contacts

Contact information is provided by the study sponsor or research team.

Charlotte E Mills, PhD

CONTACT

[email protected]

0118378 ext. 7108

Kim G Jackson, PhD

CONTACT

[email protected]

0118378 ext. 5361

Sponsors and collaborators

Lead sponsor

University of Reading

Other

Registry information

Official study title

Coffee Bioequivalence Trial: Comparing the Pharmacokinetics of Bioactive Components and Physiological Effects of Consuming Encapsulated Instant Coffee Versus Traditional Instant Coffee Brewed in Water

Important dates

Study start
2025
Primary completion
2025
Study completion
2025
First posted
Jan 3, 2025
Registry last updated
Jan 3, 2025

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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