Clinical Trials Directory

Trials / Completed

CompletedNCT05561712

Method Optimization for the Quantification of the NAD

Method Optimization for the Quantification of the NAD (Nicotinamide Adenine Dinucleotide) Metabolome in Human Whole Blood, Plasma, and Urine, and Evaluation of Baseline Inter and Intra-subject Variability

Status
Completed
Phase
Study type
Observational
Enrollment
10 (actual)
Sponsor
Société des Produits Nestlé (SPN) · Industry
Sex
All
Age
18 Years – 55 Years
Healthy volunteers
Accepted

Summary

Method optimization for the quantification of the NAD metabolome in human whole blood, and evaluation of baseline inter and intra-subject variability.

Detailed description

Whole blood from healthy participants will be collected to optimize analytical method based on liquid chromatography tandem mass spectrometry (LC-MS/MS) for the analysis of the NAD metabolome in biological samples. Parameters such as collection volume and anti-coagulants will be investigated for optimal quantification. Moreover, inter- and intra-subject variability of NAD metabolite levels in whole blood will be evaluated. Plasma and urine will also collected for method development and variability measurements.

Conditions

Interventions

TypeNameDescription
OTHERLaboratory method validationTest several sampling conditions

Timeline

Start date
2022-02-25
Primary completion
2022-03-15
Completion
2022-03-15
First posted
2022-09-30
Last updated
2022-09-30

Locations

1 site across 1 country: Switzerland

Source: ClinicalTrials.gov record NCT05561712. Inclusion in this directory is not an endorsement.

Method Optimization for the Quantification of the NAD (NCT05561712) · Clinical Trials Directory