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NCT04516213 · ClinicalTrials.gov registry record · NA

Study to Evaluate the Tolerance and Safety of a Peptide-based Enteral Formula with Partially Hydrolyzed Guar Gum (PHGG)

A NA study, sponsored by Société des Produits Nestlé (SPN).

Completed
Registry status
NA
Development phase
24
Enrollment target

NCT04516213: Completed NA study, sponsored by Société des Produits Nestlé (SPN).

NCT04516213 is a NA study that has completed, run by Société des Produits Nestlé (SPN). The registered enrollment target is 24 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT04516213, a NA study, has completed, sponsored by Société des Produits Nestlé (SPN).

COMPLETED
Registry status
NA
Development phase
24 participants
Enrollment target

Study Summary

This is a Multicenter, Open-label, Single-arm study evaluating the Tolerance and Safety of a Peptide-based Enteral Formula with Partially Hydrolyzed Guar Gum (PHGG) in the Nutritional Management of Tube-fed Children Aged 1-4 Years over a 7 day period.

Primary Outcome

Occurrence of gastrointestinal intolerance (yes/no)

Interventions

  • OTHER Enteral Formula With (PHGG)

Trial Details

FieldValue
Enrollment Target 24 participants
Start Date 2020-02-28
Est. Completion 2021-06-01
Phase NA

What the finished NCT04516213 record still lists

NCT04516213 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 24 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower).

The record links to 0 conditions, and to 1 intervention - of which Enteral Formula With (PHGG) is the first listed.

NCT04516213 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT04516213 about?

NCT04516213 is a clinical study titled "Study to Evaluate the Tolerance and Safety of a Peptide-based Enteral Formula with Partially Hydrolyzed Guar Gum (PHGG)". This is a Multicenter, Open-label, Single-arm study evaluating the Tolerance and Safety of a Peptide-based Enteral Formula with Partially Hydrolyzed Guar Gum (PHGG) in the Nutritional Management of Tube-fed Children Aged 1-4 Years over a 7 day period.

What is the current status of trial NCT04516213?

This trial is currently completed. It is a NA study. The enrollment target is 24 participants. The study started on 2020-02-28. Estimated completion is 2021-06-01.

What interventions are being tested in trial NCT04516213?

The interventions under investigation include: Enteral Formula With (PHGG) (OTHER).

Who is sponsoring clinical trial NCT04516213?

This trial is sponsored by Société des Produits Nestlé (SPN), which has 53 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT04516213's enrollment target sits among peer trials

24 1736th of 2000 higher than 246 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA 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 NCT04516213, the US trial registry maintained by the National Library of Medicine. NCT04516213 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.