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NCT06083402 · ClinicalTrials.gov registry record · NA

Efficacy of a Dietary Supplement on Parameters of Skin Aging in Men and Women

A NA study of Skin Aging, sponsored by Natals, Inc. dba Ritual.

Completed
Registry status
NA
Development phase
63
Enrollment target
1
Study location

NCT06083402 is a NA study of Skin Aging that has completed, run by Natals, Inc. dba Ritual. The registered enrollment target is 63 participants, roughly in line with the 68-participant average among 9 other Skin Aging trials with a reported enrollment target. The trial reports 1 study location across 1 state.

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The verdict

NCT06083402, a NA study of Skin Aging, has completed, sponsored by Natals, Inc. dba Ritual.

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

Study Summary

As the body ages, the skin experiences natural changes in structure and composition. These changes may manifest visibly as increased skin dryness, wrinkling, and a loss of firmness/elasticity. In this double-blind, randomized, placebo-controlled trial, the investigators will recruit healthy men and women with mild to moderate signs of skin aging and randomly assign them to either receive a HyaCera™ or placebo for 12 weeks. The investigators will perform a series of objective and subjective measurements to assess changes in skin condition. The investigators hypothesize that consumption of HyaCera™ leads to improvements in the general condition of the skin including skin hydration, crow's feet wrinkling, and other skin aging parameters.

Conditions Studied

Interventions

  • DIETARY_SUPPLEMENT Placebo
  • DIETARY_SUPPLEMENT HyaCera™

Study Locations (1)

New Jersey

  • Princeton Consumer Research - Raritan

Trial Details

FieldValue
Enrollment Target 63 participants
Start Date 2023-06-12
Est. Completion 2023-10-06
Phase NA

Sponsor

Natals, Inc. dba Ritual

1 total trials

What the Registry Record Tells You About NCT06083402

The ClinicalTrials.gov registry entry for NCT06083402 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 63 participants, a figure that helps gauge the scale of data the investigators plan to collect, roughly in line with the 68-participant average among 9 other Skin Aging trials with a reported enrollment target. The listed sponsor is Natals, Inc. dba Ritual, which has 1 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Skin Aging appearing as the primary indexed condition, and to 2 interventions - of which Placebo is the first listed.

NCT06083402 reports 1 study location spanning 1 distinct geographic area - top geographies include New Jersey.

Frequently Asked Questions

What is clinical trial NCT06083402 about?

NCT06083402 is a clinical study titled "Efficacy of a Dietary Supplement on Parameters of Skin Aging in Men and Women". As the body ages, the skin experiences natural changes in structure and composition. These changes may manifest visibly as increased skin dryness, wrinkling, and a loss of firmness/elasticity. In this double-blind, randomized, placebo-controlled trial, the investigators will recruit healthy men and ...

What is the current status of trial NCT06083402?

This trial is currently completed. It is a NA study. The enrollment target is 63 participants. The study started on 2023-06-12. Estimated completion is 2023-10-06.

What conditions does trial NCT06083402 study?

This clinical trial studies the following conditions: Skin Aging.

What interventions are being tested in trial NCT06083402?

The interventions under investigation include: Placebo (DIETARY_SUPPLEMENT), HyaCera™ (DIETARY_SUPPLEMENT).

Who is sponsoring clinical trial NCT06083402?

This trial is sponsored by Natals, Inc. dba Ritual, which has 1 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06083402 being conducted?

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

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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