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NCT04614714 · ClinicalTrials.gov registry record · Phase 2

Milk Volume Outcomes Following Oral Nicotinamide Riboside Supplementation in Mothers of Extremely Preterm Infants

A Phase 2 study, sponsored by University of California, Davis.

Not yet
Registry status
Phase 2
Development phase
40
Enrollment target

NCT04614714: Clinical Trial Phase 2 study, sponsored by University of California, Davis.

NCT04614714 is a Phase 2 study that has not yet begun recruiting, run by University of California, Davis. The registered enrollment target is 40 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (70% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT04614714, a Phase 2 study, has not yet begun recruiting, sponsored by University of California, Davis.

NOT YET RECRUITING
Registry status
Phase 2
Development phase
40 participants
Enrollment target

Study Summary

This study aims to evaluate the feasibility and effects of nicotinamide riboside (NR) supplementation in lactating mothers of infants expected to be hospitalized in the neonatal intensive care unit (NICU) for at least four weeks.

Primary Outcome

Proportion of eligible mothers who consent to enrollment in the study.

Interventions

  • OTHER Placebo
  • OTHER Nicotinamide Riboside (NR)

Trial Details

FieldValue
Enrollment Target 40 participants
Start Date 2026-06-01
Est. Completion 2026-06-30
Phase Phase 2
University of California, Davis

657 total trials

What is known before NCT04614714 opens enrollment

NCT04614714 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 40 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (70% lower).

The record links to 0 conditions, and to 2 interventions - of which Placebo is the first listed.

NCT04614714 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT04614714 about?

NCT04614714 is a clinical study titled "Milk Volume Outcomes Following Oral Nicotinamide Riboside Supplementation in Mothers of Extremely Preterm Infants". This study aims to evaluate the feasibility and effects of nicotinamide riboside (NR) supplementation in lactating mothers of infants expected to be hospitalized in the neonatal intensive care unit (NICU) for at least four weeks.

What is the current status of trial NCT04614714?

This trial is currently not yet recruiting. It is a Phase 2 study. The enrollment target is 40 participants. The study started on 2026-06-01. Estimated completion is 2026-06-30.

What interventions are being tested in trial NCT04614714?

The interventions under investigation include: Placebo (OTHER), Nicotinamide Riboside (NR) (OTHER).

Who is sponsoring clinical trial NCT04614714?

This trial is sponsored by University of California, Davis, which has 657 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT04614714's enrollment target sits among peer trials

40 1362nd of 2000 higher than 542 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 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 NCT04614714, the US trial registry maintained by the National Library of Medicine. NCT04614714 (small enrollment · none site footprint · not yet recruiting) retrieved and formatted by PlainTrial, see methodology.