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NCT04271735 · ClinicalTrials.gov registry record · NA

Pilot Study to Evaluate the Effect of Nicotinamide Riboside on Immune Activation in Psoriasis

A NA study of Obesity and Psoriasis, sponsored by National Heart, Lung, and Blood Institute (NHLBI).

Completed
Registry status
NA
Development phase
29
Enrollment target
1
Study location

NCT04271735: Completed NA study of Obesity and Psoriasis, sponsored by National Heart, Lung, and Blood Institute (NHLBI).

NCT04271735 is a NA study of Obesity and Psoriasis that has completed, run by National Heart, Lung, and Blood Institute (NHLBI). The registered enrollment target is 29 participants, below the 819-participant average among 1,053 other Obesity trials with a reported enrollment target (96% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT04271735, a NA study of Obesity and Psoriasis, has completed, sponsored by National Heart, Lung, and Blood Institute (NHLBI).

COMPLETED
Registry status
NA
Development phase
29 participants
Enrollment target
1
Study location

Study Summary

Background: Psoriasis causes chronic inflammation in the body. Researchers want to see if a kind of vitamin B3 dietary supplement can help. This might lead to more treatment options. Objective: To test if the dietary supplement nicotinamide riboside can improve immune system function in the blood and skin of people with mild to moderate psoriasis. Eligibility: People ages 18-80 with mild to moderate active psoriasis not currently treated with biological therapy Design: Participations will be screened with: * Medical and medication history * Physical exam * Measure of body mass index * Skin exam * Blood and urine tests Participants will have visit 1. They will have repeats of the screening tests. They may also have 2 skin biopsies, which are optional. These will be from both lesions and unaffected areas. The areas will be injected with a numbing medicine. A round cutting device will remove small pieces of skin from each area. Participants will take the study supplement or a placebo starting at the first visit. Neither participants nor the study team will know which they receive. Participants will take capsules twice daily for a total of 4 weeks. Participants will then have visit 2. This will include the tests performed at visit 1. Participants may by contacted by phone or email between visits to see how they are doing. If participants develop any side effects in the 7 days after they stop taking the capsules, they may have another visit.

Primary Outcome

Mean change in the TH17 cell cytokine IL-17 secretion in response to T-cell differentiation comparing the baseline versus NR or placebo.

Interventions

  • OTHER Placebo
  • DIETARY_SUPPLEMENT Niagen

Study Locations (1)

Maryland

  • National Institutes of Health Clinical Center - Bethesda

Trial Details

FieldValue
Enrollment Target 29 participants
Start Date 2020-08-26
Est. Completion 2022-12-19
Phase NA

What the finished NCT04271735 record still lists

NCT04271735 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 29 participants, a relatively small participant target, below the 819-participant average among 1,053 other Obesity trials with a reported enrollment target (96% lower).

The record links to 5 conditions, with Obesity appearing as the primary indexed condition, and to 2 interventions - of which Placebo is the first listed.

NCT04271735 reports a single indexed study location in Maryland.

Frequently Asked Questions

What is clinical trial NCT04271735 about?

NCT04271735 is a clinical study titled "Pilot Study to Evaluate the Effect of Nicotinamide Riboside on Immune Activation in Psoriasis". Background: Psoriasis causes chronic inflammation in the body. Researchers want to see if a kind of vitamin B3 dietary supplement can help. This might lead to more treatment options. Objective: To test if the dietary supplement nicotinamide riboside can improve immune system function in the blood...

What is the current status of trial NCT04271735?

This trial is currently completed. It is a NA study. The enrollment target is 29 participants. The study started on 2020-08-26. Estimated completion is 2022-12-19.

What conditions does trial NCT04271735 study?

This clinical trial studies the following conditions: Obesity, Psoriasis, Dyslipidemia, Atherosclerotic Cardiovascular Disease, Cardiometabolic Diseases.

What interventions are being tested in trial NCT04271735?

The interventions under investigation include: Placebo (OTHER), Niagen (DIETARY_SUPPLEMENT).

Who is sponsoring clinical trial NCT04271735?

This trial is sponsored by National Heart, Lung, and Blood Institute (NHLBI), which has 501 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT04271735 being conducted?

This trial has 1 study location across Maryland. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Obesity

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT04271735's enrollment target sits among peer trials

29 882nd of 1053 higher than 169 of 1,053 other Obesity trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Obesity trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT04271735, the US trial registry maintained by the National Library of Medicine. NCT04271735 (small enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.