Evidence map›Paper›PMID 41422283›Full record

Trial reportScientific reports2025

Oral sodium hyaluronate improves skin hydration, barrier function and signs of aging: a randomized, double-blind, placebo-controlled trial in 150 healthy adults.

Iva Dolečková, Pavel Kušnierik, Vratislav Berka, Matěj Šimek, Ilona Matějková, Filip Prokopec, Petra Ovesná

Registry-linked trialAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT07065110 (A Single-center, Double-blind, Randomized, Parallel-group, Placebo-controlled Study to Evaluate the Superiority of Peroral Sodium Hyaluronate to Placebo in Improving the Skin Hydration), which is not on this map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT07065110 nacompletednot on this map

A Single-center, Double-blind, Randomized, Parallel-group, Placebo-controlled Study to Evaluate the Superiority of Peroral Sodium Hyaluronate to Placebo in Improving the Skin Hydration

TypeinterventionalSponsorContipro Pharma a.s.Ran2024 to 2024Enrolled150ConditionsSkin ConditionsArmsBlood draw for the laboratory assessment, Skin test panel, HA gel, Xanthan gum
3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Iva DolečkováContipro a.s., Dolní Dobrouč 401, Dolní Dobrouč, 561 02, Czech Republic. iva.doleckova@contipro.com.
Pavel KušnierikContipro a.s., Dolní Dobrouč 401, Dolní Dobrouč, 561 02, Czech Republic.
Vratislav BerkaContipro a.s., Dolní Dobrouč 401, Dolní Dobrouč, 561 02, Czech Republic.
Matěj ŠimekContipro a.s., Dolní Dobrouč 401, Dolní Dobrouč, 561 02, Czech Republic.
Ilona MatějkováContipro a.s., Dolní Dobrouč 401, Dolní Dobrouč, 561 02, Czech Republic.
Filip ProkopecContipro a.s., Dolní Dobrouč 401, Dolní Dobrouč, 561 02, Czech Republic.
Petra OvesnáInstitute of Biostatistics and Analyses, Faculty of Medicine, Masaryk University, Brno, Czech Republic.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Oral hyaluronan has been reported to improve various aspects of skin physiology, but existing trials often lack methodological rigor, comprehensive outcome assessment, and diverse populations. This randomized, double-blind, placebo-controlled trial evaluated the effects of sodium hyaluronate (SH) supplementation at two daily doses on skin parameters in healthy Caucasian adults. A total of 150 participants were randomized to receive SH (1.8 MDa) at 60 mg/day (SH60), 120 mg/day (SH120), or placebo for 12 weeks. Facial hydration, transepidermal water loss (TEWL), sebum, elasticity, wrinkle depth, skin gloss, colorimetric parameters, epidermal thickness, dermal density, red areas, and pore size were assessed at baseline and monthly. Subjective skin condition was evaluated every two weeks, and components of natural moisturizing factor (NMF) in forearm skin were quantified by LC-MS/MS. SH120 significantly enhanced skin hydration and elasticity, while reducing TEWL, sebum, and periorbital wrinkle depth versus placebo. It also improved skin structure by increasing epidermal thickness, dermal density, and NMF levels. SH60 showed similar but more modest effects. No changes were observed for colorimetric parameters, red areas, pore size, or gloss. In conclusion, oral SH supplementation improved multiple aspects of skin physiology, supporting its use as a functional food ingredient with measurable benefits for skin health and healthy aging.Trial registration: ClinicalTrials.gov, NCT07065110 (retrospectively registered on 15 Jul 2025); EFSA (European Food Safety Authority) registry: EFSA202400027979 (prospectively filed on 06 Jun 2024).

Indexed as

Hyaluronic AcidSkinSkin AgingAdministration, OralAdultDouble-Blind MethodElasticityFemaleHealthy VolunteersHumansMaleMiddle AgedWater Loss, InsensibleYoung AdultHyaluronic AcidNutraceuticalOral sodium hyaluronateRandomized controlled trialSkin hydrationTransepidermal water lossWrinkles

Identifiers

PMID41422283
PMCPMC12827323

What Socratic holds

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LicenceCC BY
Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.