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NCT07065110

The Effect of Peroral Sodium Hyaluronate on the Skin

Completed NA Last updated 15 July 2025
What this trial tests

NA trial testing Blood draw for the laboratory assessment in Skin Conditions in 150 participants. Completed in 13 December 2024.

Timeline
17 June 2024
Primary endpoint
13 December 2024
13 December 2024

Quick facts

Lead sponsorContipro Pharma a.s.
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposeprevention
Enrollment150
Start date17 June 2024
Primary completion13 December 2024
Estimated completion13 December 2024
Sites1 location across Czechia

Drugs / interventions tested

Conditions studied

Sponsor

Contipro Pharma a.s. — full company profile →

Who can join

Adults 18 to 60, any sex, with Skin Conditions. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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 and other skin-related parameters.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Oral sodium hyaluronate improves skin hydration, barrier function and signs of aging: a randomized, double-blind, placebo-controlled trial in 150 healthy adults.
    Dolečková I, Kušnierik P, Berka V, Šimek M, et al · · 2025 · PMID 41422283 · DOI 10.1038/s41598-025-32758-5

Verify or expand the search:

Other trials of Blood draw for the laboratory assessment

Trials testing the same drug.

Other recruiting trials for Skin Conditions

Currently open trials in the same condition.

Other Contipro Pharma a.s. trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT07065110.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing