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Completed

NCT Number: NCT00975351

Estimation of Plasma Folate Apparent Volume of Distribution in Adults

The aim of this study is to calculate the plasma apparent volume of distribution of natural folate to give a more accurate value for use in a mathematical model of apparent folate absorption.

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Key information

Conditions

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Institute of Food Research

Norwich, Norfolk, NR4 6JF, United Kingdom

About this study

Bioavailability is a major determinant of nutritional status. In order to determine a safe level of folate fortification, its bioavailability must be assessed, so that risk-benefit analysis can be carried out. Recently, a mathematical model of folate true absorption which takes into account the liver first pass was devised (ref 1). In this model, the volume of distribution is a convenient method for describing how well a nutrient is removed from plasma and distributed into tissues.

In this study, volume of distribution will be more accurately estimated using an intravenous dose of labelled (13C5) dose of natural folate (5-methyltetrahydrofolic acid) in healthy adults aged 18-65, over a wide body mass index (BMI) range.

Healthy adults will be given an IV dose of a small amount of 13C5 5-methyltetrahydrofolic acid, and blood samples will be taken at regular time points via a cannula over a 2hr time period.

The primary objective is to estimate the sampled plasma pool volume of distribution in order to quantify the fraction of any folate test dose, or folate metabolites, appearing in systemic plasma circulation in future studies of bioavailability.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Males and females
  • Aged 18-65
  • Body mass index above 19.5 and below 40
  • Smokers and non-smokers
  • Participation in the FolGene study

Exclusion criteria

  • Pregnancy or been pregnant in last 12 months
  • History of fits, seizures or blackouts
  • Parallel participation in other research projects which invole dietary intervention and/or sampling of biological fluids/material which study nurses advice would affect either wellbeing of volunteer or the study data, apart from participation in the FolGene study
  • Any person related to or living with a member of the study team
  • Participation in another research project which involves blood sampling within the last 4 months unless total amount blood combined from both studies is less than 470ml
  • Had donated blood within 16 weeks of starting the study
  • Prescribed medication for epilepsy/seizures
  • Diabetics
  • History of any gastrointestinal disorder requiring medical treatment
  • Any long term medical condition requiring active treatment which may affect volunteers wellbeing or the study data

Treatment and study plan

13C5-labelled 5-methyltetrahydrofolic acid

Dietary Supplement

one intravenous bolus dose of no more than 500nmole 13C5-labelled 5-methyltetrahydrofolic acid, followed by multiple blood samplings at regular time intervals. Total 2hr "intervention".

Other names: 13C5-labelled 5 methyltetrahydrofolic acid, calcium salt, 6S-5-CH3-H4-Pte[13C5] Glu-Ca

Primary outcomes

  1. Estimation of sampled plasma pool volume of distribution for natural folates

    Time frame: 2 hours

Sponsors and collaborators

Lead sponsor

Quadram Institute Bioscience

Other

Collaborators

  • University of Nottingham

Registry information

Acronym: FOLCAN

Important dates

Study start
2009
Primary completion
2009
Study completion
2010
First posted
Sep 11, 2009
Registry last updated
Feb 18, 2013

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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