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CompletedNCT07900308Updated Oct 28, 2026

A Clinical Study to Assess the Effectiveness of the Hyper Glow Serum on Skin Complexion and Hydration

An interventional study of Hyper Glow Serum in Poor Facial Skin Complexion, Skin Hydration and Skin Texture, sponsored by Dime Beauty Co.. Completed at 1 site in United States. Open to participants aged 18 Years to 65 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-10-28.

Sponsored by Dime Beauty Co. · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Registered 2 years 7 months after the study started (first participant enrolled Mar 2024, registered Oct 2026).
Updated Oct 28, 2026Newly registeredGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
35
Allocation
Not applicable
Ages
18 Years to 65 Years
Sex
All
01

Study summary

This single-group, open-label, virtual clinical trial will evaluate the effectiveness of the Hyper Glow Serum by DIME Beauty on skin complexion and hydration in 35 female participants over 60 days. Participants will apply 3-5 drops of the serum to the face and neck each morning, with assessments conducted via self-reported questionnaires, expert skin grading, and before-and-after photographs at Baseline, Day 14, Day 30, and Day 60.

The primary objective is to examine the effect of daily use of the Hyper Glow Serum on overall skin complexion, including texture, evenness, and brightness. The secondary objective is to assess changes in participants' perception of skin hydration, tightness, and youthfulness over the 60-day intervention period.

02

Conditions studied

  • Poor Facial Skin Complexion
  • Skin Hydration
  • Skin Texture
  • Skin Evenness
  • Skin Tightness
03

In context

Lead sponsor

Dime Beauty Co. is the lead sponsor of 5 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Female
  • Individuals aged 18-65
  • Individuals with no known allergies to the product ingredients
  • Individuals willing to comply with the study requirements
  • Self-reported poor facial skin complexion
  • Self-reported issues with skin hydration and tightness
  • Generally healthy - do not live with any uncontrolled chronic disease
  • Must not use any other oil-based serums for the duration of the study
  • Willing to maintain the same skincare products and routine for the duration of the study (apart from other serums)
  • Has been using the same skincare products and routine for the past month

Exclusion criteria

Exclusion Criteria:

  • Individuals with known skin conditions or diseases of the face and neck
  • Individuals currently on medication that affects skin health
  • Individuals who have undergone facial cosmetic procedures in the past six months
  • Any pre-existing chronic conditions that would prevent participants from adhering to the protocol, including oncological and psychiatric disorders
  • Women who are pregnant, breastfeeding, or trying to conceive
  • Anyone unwilling to follow the study protocol
  • Anyone currently participating or planning to participate in a research study
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
35 participants (actual)

Study arms

  • Experimental
    Hyper Glow Serum

    Dietary Supplement: Hyper Glow Serum

Interventions

  • Dietary supplementHyper Glow Serum

    All 35 enrolled female participants apply 3-5 drops of Hyper Glow Serum to the face and neck daily in the morning for 60 days. Participants cleanse (and optionally tone) before application. If irritation occurs, frequency is reduced to 3-4 times per week. Two bottles of product are provided, sufficient for the full 60-day duration.

06

What researchers measure

Primary outcomes

  1. Change in Skin Complexion (Texture)

    Self-reported questionnaire measuring participant-perceived skin texture

    Time frame: Baseline, Day 14, Day 30, and Day 60

  2. Change in Skin Complexion (Evenness)

    Self-reported questionnaire measuring participant-perceived skin evenness

    Time frame: Baseline, Day 14, Day 30, and Day 60

  3. Change in Skin Complexion (Brightness)

    Self-reported questionnaire measuring participant-perceived skin brightness

    Time frame: Baseline, Day 14, Day 30, and Day 60

  4. Expert Skin Grading of Overall Complexion

    Expert-evaluated grading of overall skin complexion assessed from participant photographs

    Time frame: Baseline, Day 30, and Day 60

Secondary outcomes

  1. Change in Self-Reported Skin Hydration

    Self-reported questionnaire measuring participant-perceived skin hydration

    Time frame: Baseline, Day 14, Day 30, and Day 60

  2. Change in Self-Reported Skin Tightness

    Self-reported questionnaire measuring participant-perceived skin tightness

    Time frame: Baseline, Day 14, Day 30, and Day 60

  3. Change in Self-Reported Skin Youthfulness

    Self-reported questionnaire measuring participant-perceived skin youthfulness

    Time frame: Baseline, Day 14, Day 30, and Day 60

  4. Expert Skin Grading of Skin Hydration

    Expert-evaluated grading of skin hydration, tightness, and youthfulness assessed from participant photographs

    Time frame: Baseline, Day 30, and Day 60

  5. Expert Skin Grading of Tightness

    Expert-evaluated grading of skin hydration, tightness, and youthfulness assessed from participant photographs

    Time frame: Baseline, Day 30, and Day 60

  6. Expert Skin Grading of Youthfulness

    Expert-evaluated grading of skin hydration, tightness, and youthfulness assessed from participant photographs

    Time frame: Baseline, Day 30, and Day 60

07

Study locations

1 site
  • Citruslabs
    Las Vegas, Nevada 89118, United States
08

Updates

1 registry update since Sep 25, 2026
Registered
First appeared on the registry. No changes since
Oct 28, 2026
Show all 1 update
  1. Oct 28, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

09

Registry details

Key details

Study ID
NCT07900308
Lead sponsor
Dime Beauty Co.
Collaborators
Citruslabs
Responsible party
Sponsor
First posted
Oct 28, 2026
Start date
Mar 1, 2024
Primary completion
May 31, 2024
Completion
May 31, 2024
Last update
Oct 28, 2026

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Oct 2026. You cannot join it, but the record below documents what was studied.

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Discussion

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