World Health Organization site
Skip Navigation Links

Main
Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: ClinicalTrials.gov
Last refreshed on: 12 December 2020
Main ID:  NCT03816020
Date of registration: 07/12/2018
Prospective Registration: Yes
Primary sponsor: Haukeland University Hospital
Public title: NAD-supplementation in Drug naïve Parkinson's Disease NAD-PARK
Scientific title: NAD-PARK: A Double-blinded Randomized Pilot Trial of NAD-supplementation in Drug naïve Parkinson's Disease
Date of first enrolment: March 9, 2019
Target sample size: 30
Recruitment status: Completed
URL:  https://clinicaltrials.gov/show/NCT03816020
Study type:  Interventional
Study design:  Allocation: Randomized. Intervention model: Parallel Assignment. Primary purpose: Basic Science. Masking: Triple (Participant, Care Provider, Investigator).  
Phase:  N/A
Countries of recruitment
Norway
Contacts
Name:     Charalampos Tzoulis, PhD
Address: 
Telephone:
Email:
Affiliation:  Nevro-Sysmed
Key inclusion & exclusion criteria

Inclusion Criteria:

1. Newly diagnosed with PD

2. Drug naïve with respect to dopaminergic treatment

3. Have a clinical diagnosis of idiopathic PD according to the MDS clinical diagnostic
criteria for PD

Exclusion Criteria:

1. [¹²³I]FP-CIT single photon emission CT (DaTscan) does not show nigrostriatal
degeneration.

2. Magnetic resonance imaging (MRI) suggestive of atypical parkinsonsism.

3. Dementia or other neurological disorder at baseline visit

4. Metabolic, neoplastic, or other physically or mentally debilitating disorder at
baseline visit



Age minimum: 18 Years
Age maximum: N/A
Gender: All
Health Condition(s) or Problem(s) studied
Parkinson Disease
Neurodegenerative Diseases
Intervention(s)
Other: Placebo
Dietary Supplement: Nicotinamide Riboside
Primary Outcome(s)
PDRP changes from NR use [Time Frame: 4 weeks]
Secondary Outcome(s)
Motoric change of symptoms from NR use [Time Frame: 4 weeks]
Secondary ID(s)
2018/597
Source(s) of Monetary Support
Please refer to primary and secondary sponsors
Secondary Sponsor(s)
Ethics review
Results
Results available:
Date Posted:
Date Completed:
URL:
Disclaimer: Trials posted on this search portal are not endorsed by WHO, but are provided as a service to our users. In no event shall the World Health Organization be liable for any damages arising from the use of the information linked to in this section. None of the information obtained through use of the search portal should in any way be used in clinical care without consulting a physician or licensed health professional. WHO is not responsible for the accuracy, completeness and/or use made of the content displayed for any trial record.
Copyright - World Health Organization - Version 3.6 - Version history