A Comparison of Three Commercial Oral Rehydration Solutions Consumed After Extra-cellular Dehydration
Study Details
Study Description
Brief Summary
Dehydration is commonplace in a number of settings, including exercise, daily living (i.e. inadequate fluid intake) and with relatively common bacterial/viral infections that induce diarrhoea and/or vomiting. As such, it is important to develop effective strategies to facilitate the recovery and maintenance of body water (i.e. rehydration). Whilst rehydration from exercise dehydration has been well-studied, rehydration from other types of dehydration have not. Despite this, oral rehydration solutions have been produced and are commercially available (in chemists/pharmacies and supermarkets) to help recover from dehydration produced by illnesses like diarrhoea and vomiting. Most commercially available oral rehydration solutions use a sugar-base (glucose) and a mixture of electrolytes, but little work has gone into evaluating the efficacy of such solutions. Furthermore, more recent work has explored the use of proteins that they may offer some advantage over sugar/glucose-based beverages.
Therefore, the aim of this study is to investigate the efficacy of a protein-based oral rehydration solution compared to two current commercially available glucose-based oral rehydration solutions.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
N/A |
Detailed Description
Dehydration refers to a decrease in body water and occurs when water losses in urine, sweat or other body fluid secretions (e.g vomit or diarrhoea) exceed fluid intake in drinks and foods. Indeed, dehydration is commonplace in a number of settings, including exercise, daily living (i.e. inadequate fluid intake) and with relatively common bacterial/viral infections that induce diarrhoea and/or vomiting. As such it is important to develop effective strategies to facilitate the recovery and maintenance of body water (i.e. rehydration).
Whilst rehydration from exercise dehydration has been well-studied, rehydration from other types of dehydration have not. Despite this, oral rehydration solutions have been produced and are commercially available (in chemists/pharmacies and supermarkets) to help recover from dehydration produced by illnesses like diarrhoea and vomiting. Oral rehydration solutions have been developed that vary in their composition for both electrolytes and other nutrients (glucose, amino acids etc.). Most commercially available oral rehydration solutions use a sugar-base (glucose) and a mixture of electrolytes, but little work has gone into evaluating the efficacy of such solutions. Furthermore, more recent work has explored the use of amino acids (the building blocks of proteins) in isolation or as complete proteins and suggest that they may offer some advantage over sugar/glucose-based beverages.
Dehydration produced by illnesses like diarrhoea and vomiting cause water an electrolyte losses that are different in nature to exercise and as such, exercise is not a good way to study these effects. The type of dehydration produced with diarrhoea and vomiting can be mimicked by using a diuretic like furosemide. This type of diuretic is used clinically in situations of water overload (e.g. congestive heart failure or high blood pressure) and are used daily for months in many patients. They produce mild dehydration (~2-2.5%) and thus offer the opportunity to understand recovery from the type of dehydration caused by illness, without the presence of illness.
Given the body water contains high amounts of salts (electrolyte), when dehydration occurs electrolytes are also lost from the body. These electrolytes are needed to retain water in the various spaces of the body (inside cells, in the blood etc.) and thus failure to replace the electrolytes lost during dehydration will lead to a less effective rehydration response. Therefore, commercial oral rehydration solutions contain a balance of different electrolytes to replace those lost with dehydration and to help retain the ingested fluid. However, different formulations use a different balance of electrolytes and little work has examined the efficacy of these different formulations.
Therefore there is a need to understand the efficacy of different oral rehydration solution formulations following dehydration, something that has received little attention to date, surprisingly. Therefore, this study will compare the rehydration efficacy of a commercial amino-acid based oral rehydration solution compared to two current commercially available glucose-based oral rehydration solutions after dehydration induced by a diuretic.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: Commercially Available Oral Rehydration Solution A A commercially available oral rehydration solution (~2.8% carbohydrate, ~45 mmol/L sodium, ~20 mmol/L potassium, 34 mmol/L chloride) |
Other: Composition of oral rehydration solutions
Investigate the efficacy of an amino acid-based oral rehydration solution compared to two current commercially available glucose-based oral rehydration solutions.
|
| Experimental: Commercially Available Oral Rehydration Solution B A commercially available oral rehydration solution (~0.1% carbohydrate, ~2% amino acids (protein), ~67 mmol/L sodium, ~20 mmol/L potassium, 30 mmol/L chloride) |
Other: Composition of oral rehydration solutions
Investigate the efficacy of an amino acid-based oral rehydration solution compared to two current commercially available glucose-based oral rehydration solutions.
|
| Experimental: Commercially Available Oral Rehydration Solution C A commercially available oral rehydration solution (~2.2% carbohydrate, ~45 mmol/L sodium, ~20 mmol/L potassium) |
Other: Composition of oral rehydration solutions
Investigate the efficacy of an amino acid-based oral rehydration solution compared to two current commercially available glucose-based oral rehydration solutions.
|
Outcome Measures
Primary Outcome Measures
- Net fluid balance [9 hours]
Determined from urine output and drink volume collected before and after drink ingestion
- Drink retention [4 hours]
Determined from urine output and drink volume collected before and after drink ingestion
- Electrolyte balance [9 hours]
Determined from electrolyte concentrations (i.e., sodium, potassium, chloride) in urine and drink samples before and after drink ingestion
- Speed of rehydration [4 hours]
Determined from urine output and drink volume collected before and after drink ingestion
Secondary Outcome Measures
- Plasma volume [9 hours]
Determined from haemoglobin and haematocrit measures in blood samples collected before and after drink ingestion
- Plasma osmolality [9 hours]
Determined from venous blood samples collected before and after drink ingestion
- Urine volume [9 hours]
Determined from urine samples collected before and after drink ingestion
- Urine electrolyte concentration (i.e., sodium, potassium, chloride) [9 hours]
Determined from urine samples collected before and after drink ingestion
- Blood electrolyte concentration (i.e., sodium, potassium, chloride) [9 hours]
Determined from blood samples collected before and after drink ingestion
- Body mass change [9 hours]
Determined from weighing participants before and after drink ingestion
- Urine specific gravity [9 hours]
Determined from urine samples collected before and after drink ingestion
Eligibility Criteria
Criteria
Inclusion Criteria:
-
18-45 years of age
-
male or female
-
good health
Exclusion Criteria:
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Gastrointestinal, cardiovascular or renal conditions; other health conditions that might influence the study outcomes.
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Medication use (e.g. anti-biotics, diuretics, NSAIDS etc.) that might influence the study outcomes or interact with furosemide.
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Allergy to sulfonamides (sulfa drugs).
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Smoking (including vaping)
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Amenorrhoeic females
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Any high-level/elite athlete, or aspiring high level athlete, where drug testing/regulations are carried out and regulations need to be followed (furosemide is prohibited in sport as it is used as a masking agent).
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Loughborough University | Loughborough | Leicestershire | United Kingdom | LE11 3TU |
Sponsors and Collaborators
- Loughborough University
- entrinsic bioscience LLC
Investigators
None specified.Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- LEON8472