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Postprandial Response of Individuals to Dietary Inorganic Phosphate

Postprandial Response of Individuals to Dietary Inorganic Phosphate- a Randomized Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03771924
Enrollment
29
Registered
2018-12-11
Start date
2018-08-16
Completion date
2020-01-20
Last updated
2020-05-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cardiovascular Risk Factor

Keywords

inorganic phosphate, postprandial response, fibroblast growth factor-23, health individuals

Brief summary

The study aims to compare the postprandial response of plasma phosphate and cardiometabolic relevant factors to phosphate intake in defined diet(s).

Detailed description

It is a monocentric, controlled intervention trial. The study will be carried out in cross-over design. This design was chosen because of a moderately strong individual metabolic response to the test meal. Two interventions are planned in which the subjects will receive a test meal with phosphate supplement or with placebo in random order on 2 days. Subjects will be randomized to one of the 2 treatment arms. On the two intervention days (T1 and T2), the subjects are placed a venous indwelling cannula. Immediately after the first blood sample the subjects take the fat and carbohydrate-rich test meal along with 700 mg of phosphorus or a placebo, both in the form of capsules. Phosphorus is administered as sodium phosphate . The placebo used is sodium chloride with equivalent amounts of sodium. The filler should be silica and mannitol. The capsules are made of hard gelatin and dissolve in about 10 minutes. The capsules are taken with 300 ml of water. The verum and placebo capsules are produced by the central pharmacy of the University Hospital. The test meal consists of a pasta dish with oily tomato sauce. It is freshly prepared by the study staff and packaged airtight in individual portions before being handed out to the subjects. The test meal should be consumed within 10 - 12 minutes. The time is documented by the study staff. The next blood sample is taken immediately after the end of consumption (time 0), all other 15, 30, 45, 60, 90, 120, 180, 240, 300, 360, 420 and 480 minutes thereafter. All blood samples are taken in a lying position. The first 3 hours after eating the test meal the subjects should spend reclining. In the following 5 hours subjects are free to move in the study center with each patient taking a recumbent position 10 minutes before the next blood draw. Immediately before all blood samples are taken the measurement of blood pressure and pulse is provided for which the opposite arm is to be used. Furthermore the collection of urine samples is provided every hour. Subjects are encouraged to take 200 ml of water every hour on the intervention day. At the end of the intervention, a snack will be provided.

Interventions

DIETARY_SUPPLEMENTinorganic phosphate

Sodium phosphate

DIETARY_SUPPLEMENTplacebo

Sodium chlorid

Sponsors

German Federal Ministry of Education and Research
CollaboratorOTHER_GOV
Martin-Luther-Universität Halle-Wittenberg
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
Yes

Inclusion criteria

* healthy men and women * age between 18 and 60 years * informed consent * body mass index between 18,5 up to 29,9 kg/m2 * anamnesis without diagnostic findings

Exclusion criteria

* Participants with epidermal growth factor receptor (eGFR) \< 90 ml/min and chronic kidney disease * Subjects suffering from vitamin D-deficiency (plasma 25(OH)D \< 30 nmol/l) * Pregnancy or lactation * Subjects with any acute or chronic diseases (infection, tumor, cardiovascular diseases, respiratory diseases, inflammatory diseases), gastrointestinal diseases, diabetes mellitus type 1 and 2, bone diseases, diseases of the parathyroid gland * Use of medication * Use of dietary supplements (minerals) * Relevant food allergies (wheat protein, tomatoes) * Weight reduction * Smokers * Blood donor in the last 3 months * Participation in another intervention study

Design outcomes

Primary

MeasureTime frameDescription
Postprandial change of plasma phosphate concentration from baseline (0 minute) until 480 minutes0,15,30,45,60,90,120,180,240,300, 360, 420 and 480 minutes after ingestion of testmeal rich in carbohydrates and fatImpact of inorganic phosphate on the postprandial levels of plasma phosphate concentration

Secondary

MeasureTime frameDescription
Postprandial course of the plasma concentration of: phosphate status markers (c-terminal and intact FGF23, parathormone, soluble Klotho (sKlotho), calcitriol)0,15,30,45,60,90,120,180,240,300, 360, 420 and 480 minutes after ingestion of testmeal rich in carbohydrates and fatImpact of inorganic phosphate on the postprandial levels
Postprandial course of plasma concentration of: cardiovascular risk marker glucose0,15,30,45,60,90,120,180,240,300, 360, 420 and 480 minutes after ingestion of testmeal rich in carbohydrates and fatImpact of inorganic phosphate on the postprandial levels
Postprandial course of plasma concentration of: cardiovascular risk marker insulin0,15,30,45,60,90,120,180,240,300, 360, 420 and 480 minutes after ingestion of testmeal rich in carbohydrates and fatImpact of inorganic phosphate on the postprandial levels
heart rate0,15,30,45,60,90,120,180,240,300, 360, 420 and 480 minutes after ingestion of testmeal rich in carbohydrates and fattime course: measurement of heart rate in beats per minute
Postprandial course of plasma concentration of: cardiovascular risk marker triglycerides0,15,30,45,60,90,120,180,240,300, 360, 420 and 480 minutes after ingestion of testmeal rich in carbohydrates and fatImpact of inorganic phosphate on the postprandial levels
Postprandial course of the plasma concentration of: electrolytes (calcium, sodium, potassium, magnesium)0,15,30,45,60,90,120,180,240,300, 360, 420 and 480 minutes after ingestion of testmeal rich in carbohydrates and fatImpact of inorganic phosphate on the postprandial levels
Postprandial course of concentration of: calcification markers dephosphorylated, noncarboxylated matrix Gla protein (dp-ucMGP), fetuin A, osteocalcin, osteoprotegerin) Inflammatory markers (hsCRP and inflammatory cytokines, especially interleukin (IL-1β)0,15,30,45,60,90,120,180,240,300, 360, 420 and 480 minutes after ingestion of testmeal rich in carbohydrates and fatImpact of inorganic phosphate on the postprandial levels
Activation of NLRP3-inflammasome components (ASC, caspase-1) in isolated peripheral blood monocytes (PBMC) and granulocytes under basal conditions and after stimulation0,15,30,45,60,90,120,180,240,300, 360, 420 and 480 minutes after ingestion of testmeal rich in carbohydrates and fatImpact of inorganic phosphate on the postprandial levels
systolic and diastolic blood pressures0,15,30,45,60,90,120,180,240,300, 360, 420 and 480 minutes after ingestion of testmeal rich in carbohydrates and fattime course: measurement of blood pressure in mm Hg
Postprandial course of urine concentrations of electrolytes (phosphate, sodium, potassium, calcium, magnesium) and creatinine0,15,30,45,60,90,120,180,240,300, 360, 420 and 480 minutes after ingestion of testmeal rich in carbohydrates and fatImpact of inorganic phosphate on the postprandial levels
Postprandial course of plasma concentration of: cardiovascular risk marker cholesterol0,15,30,45,60,90,120,180,240,300, 360, 420 and 480 minutes after ingestion of testmeal rich in carbohydrates and fatImpact of inorganic phosphate on the postprandial levels

Countries

Germany

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 7, 2026