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
| Type | Name | Description |
|---|---|---|
| OTHER | Laboratory method validation | Test 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.