Poitiers University Hospital
Poitiers, 86021, France
NCT Number: NCT01532401
The primary objective of this study is to analyze the sensitivity of blood pressure to oral salt intake. Matched male and female participants will be selected as normal weight, overweight, and obese.
Participating subjects will have a first visit with blood pressure measurement and a blood sample. In two consecutive phases of one week, subjects will receive 12 pills of sodium (6 grams) or corresponding placebo. Blood pressure will be measured at the end of each phase.
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Notify Me6 year–45 year
All sexes
Interventional
Phase 2
Poitiers, 86021, France
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
sodium chloride 500mg
Methylcellulose 37 ml
Poitiers University Hospital
Other
Simplification of the Test of Sensibility in the Salt: Preliminary Study at the Child and the Adult
Acronym: PLADSEL
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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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