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Clinical Trials/NCT00890487
NCT00890487UnknownNot Applicable

Effects of Hyaluronic Acid Oral Supplementation on the Vaginal Epithelium: a Prospective, Randomized, Double-Blind, Placebo Controlled Study

University of Messina1 site in 1 country70 target enrollmentStarted: May 1, 2009Last updated:
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Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Enrollment
70
Locations
1
Primary Endpoint
effects of the oral somministration hyaluronic acid in menopause women with vaginal distress
Study OverviewStudy DesignEligibility CriteriaArms & InterventionsOutcomesInvestigatorsSitesRecords & IdentifiersSimilar Trials

Study Overview

Brief Summary

The purpose of this trial is to study the effects of the oral supplementation hyaluronic acid in menopause women with vaginal distress for treatment vaginal distress.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Double (Participant, Care Provider)

Eligibility Criteria

Ages
45 Years to 60 Years (Adult)
Sex
Female
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •menopause
  • •vaginal distress
  • •no other therapy

Exclusion Criteria

  • •vaginal infection
  • •Sjogren Syndrome

Arms & Interventions

hyaluroni acid pill

Other

Intervention: hyaluronic acid pill (Other)

Outcomes

Primary Outcomes

effects of the oral somministration hyaluronic acid in menopause women with vaginal distress

Time Frame: three months

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other

Study Sites (1)

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