Trials / Unknown
UnknownNCT02950441
Nicotinamide Adenine Dinucleotide and Skeletal Muscle Metabolic Phenotype
Nicotinamide Adenine Dinucleotide and Skeletal Muscle Metabolic Phenotype (NADMet)
- Status
- Unknown
- Phase
- Phase 2
- Study type
- Interventional
- Enrollment
- 12 (estimated)
- Sponsor
- University of Birmingham · Academic / Other
- Sex
- Male
- Age
- 70 Years – 80 Years
- Healthy volunteers
- Accepted
Summary
This study is designed to assess the physiological consequences of elevating Nicotinamide Adenine Dinucleotide (NAD+) availability using Nicotinamide Riboside (NR) supplementation in skeletal muscle tissue, and examine its effect upon muscle metabolic phenotype.
Detailed description
-NAD+ sensitive metabolic decline in ageing, including sarcopenia, leads to a reduction in energy metabolism, contribute to chronic inflammation, disposing individuals to metabolic disease and overall decreased later-life health. Prominent metabolic changes include a decline in NAD+ content and deterioration in muscle NAD+ mediated signalling and mitochondrial function, ultimately compromising skeletal muscle and whole body energy homeostasis. The most efficient means to boost NAD+ in muscle appears to be oral delivery of NR, and participants will be supplemented with 1000mg NR (2x x250mg tablets twice daily) for 3 weeks. * Hypothesis: elevating skeletal muscle NAD+ bioavailability using NR supplementation will increase markers of mitochondrial function and that will manifest as a more favourable metabolic profile. * Study Setting: the study will be carried out at the NIHR/Wellcome Trust Clinical Research Facility, Queen Elizabeth Hospital Birmingham.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DIETARY_SUPPLEMENT | Nicotinamide Riboside | |
| OTHER | Placebo |
Timeline
- Start date
- 2016-06-01
- Primary completion
- 2018-09-01
- Completion
- 2019-09-01
- First posted
- 2016-11-01
- Last updated
- 2017-06-07
Locations
1 site across 1 country: United Kingdom
Source: ClinicalTrials.gov record NCT02950441. Inclusion in this directory is not an endorsement.