Buoy Electrolyte Study on Hydration Status of Active Men and Women
Completed · Not applicable
Conditions studied: Dehydration, Electrolyte Imbalance, Electrolyte Depletion, Fluid and Electrolyte Imbalance
In brief
Buoy is an all-natural, organic, FDA compliant dietary electrolyte supplement that can be dissolved in 8-12oz water (or other liquid) and provide electrolytes in servings of 1/3 teaspoon. This study will evaluate Buoy in hydrating active adults.
Key facts
- Study ID
- NCT05768789
- Run by
- University of Pittsburgh
- People needed
- 30
- Starts
- 2023-09-13
- Expected to finish
- 2024-04-27
- Last updated by the study team
- 2025-05-14
Who can join
Age: 18 and older, up to 45. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Male or female, >18 to 45 years of age
- Freely given written consent
- Non-tobacco users
- Negative pregnancy test in women of childbearing potential
- BMI < 35 kg/m2
- GFR > 60 ml/min
- No known underlying medical condition
- Willing to refrain from EtOH for 24h prior to test day
- Willing to refrain from strenuous exercise for 24 h prior to each test day
- Acceptable to have one 8oz cup of coffee/liquid on the morning of the test, but must be consistent each visit
- Without active infection of any kind
- Engaged in exercise three or more hours per week
You may not qualify if…
- Abnormal creatinine (Cr > 1.2).
- Proteinuria / hematuria / glucosuria based on urine dipstick.
- Diagnosed medical condition that would impede results (CHF, HTN, CAD, CKD, history of electrolyte abnormality).
- Pregnancy
- Use of diuretics within past 2 weeks
- Obesity (BMI > 35)
- Active infection based on symptoms (bacterial or viral)
- Hemodynamic abnormality at screening visit: Blood pressure less than 100/60 or greater than 140/90.
Where it is running
- UPMC Montefiore Hospital — Pittsburgh, Pennsylvania, United States
- UPMC Presbyterian — Pittsburgh, Pennsylvania, United States
Full record on ClinicalTrials.gov
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