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NCT03568968CompletedPhase 3

A Randomized Controlled Trial of Nicotinamide Riboside Supplementation in Early Parkinson's Disease

A Randomized Controlled Trial of Nicotinamide Riboside Supplementation in Early Parkinson's Disease: the NOPARK Study

Source: ClinicalTrials.gov · Last updated 26 Sept 2025

Brief summary (registry, in English)

NOPARK is a double-blinded randomized controlled phase II trial, with the aim to assess the efficacy of nicotinamide adenine dinucleotide (NAD)-replenishment therapy in the form of oral nicotinamide riboside (NR) in delaying the progression of early Parkinson's disease (PD). A total of 400 persons with early stage Parkinson's disease will be enrolled, randomized on nicotinamide riboside (NR) 500mg x 2 per day or placebo, and followed for 52 weeks.

Status (registry)
Completed
Phase (registry)
Phase 3
Study type
Interventional
Enrollment
410 (actual)
First submitted
14 Jun 2018
Start date
6 May 2020
Primary completion date
17 Jun 2025
Lead sponsor
Haukeland University Hospital
NCT number
NCT03568968

What you commit to

  • Study type: Interventional · Phase 3
  • Participants enrolled: 410
  • From 6 May 2020 to the primary completion date, 17 Jun 2025
  • 11 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Dementia or other neurodegenerative disorder at baseline visit
  • Any psychiatric disorder that would interfere with compliance in the study.
  • Any severe somatic illness that would make the individual unable to comply and participate in the study.
  • Metabolic, neoplastic, or other physically or mentally debilitating disorder at baseline visit.
  • Genetically confirmed mitochondrial disease

Other

  • Diagnosed with atypical parkinsonism or vascular parkinsonism
  • Use of high dose vitamin B3 supplementation within 30 days of enrolment

Who the study is looking for

  • Have a clinical diagnosis of idiopathic PD according to the MDS clinical diagnostic criteria for Parkinson's disease
  • \[¹²³I\]FP-CIT single photon emission CT (DaTscan) confirming nigrostriatal degeneration
  • Diagnosed with PD within 2 years from enrolment
  • Hoehn and Yahr score \< 3 at enrolment
  • Optimal symptomatic therapy, not requiring adjustments, for at least 1 month.
  • Age equal to or greater than 35 years at time of enrolment.

Age in the registry: 35 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (11)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Arendal Hospital
Coordinator of this site? Confirm its status
ArendalNorwayUnknown status
Haukeland University Hospital
Coordinator of this site? Confirm its status
BergenNorwayUnknown status
Bodø Hospital
Coordinator of this site? Confirm its status
BodøNorwayUnknown status
Vestre Viken Hospital
Coordinator of this site? Confirm its status
DrammenNorwayUnknown status
Førde sykehus
Coordinator of this site? Confirm its status
FørdeNorwayUnknown status
Østfold Hospital
Coordinator of this site? Confirm its status
FredrikstadNorwayUnknown status
Haugesund Hospital
Coordinator of this site? Confirm its status
HaugesundNorwayUnknown status
Molde Sjukehus
Coordinator of this site? Confirm its status
MoldeNorwayUnknown status
Oslo University Hospital
Coordinator of this site? Confirm its status
OsloNorwayUnknown status
Akershus University Hospital
Coordinator of this site? Confirm its status
OsloNorwayUnknown status
University Hospital of North Norway
Coordinator of this site? Confirm its status
TromsøNorwayUnknown status

Related publications

This page is information, not medical advice. Discuss any trial with your doctor.