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Active Not RecruitingNCT07367061

Clinical Investigation to Assess Safety and Efficacy of INNEA AQUA in Adult Women With Vulvo-Vaginal Atrophy (VVA)

Status
Active Not Recruiting
Phase
N/A
Study type
Interventional
Enrollment
62 (actual)
Sponsor
Innate srl · Industry
Sex
Female
Age
18 Years – 75 Years
Healthy volunteers
Not accepted

Summary

Clinical investigation to assess safety and efficacy of INNEA AQUA in adult women with Vulvo-Vaginal Atrophy (VVA). To assess the Safety and efficacy of INNEA AQUA

Detailed description

Clinical investigation to assess safety and efficacy of INNEA AQUA in adult women with Vulvo-Vaginal Atrophy (VVA). To assess the Safety and efficacy of INNEA AQUA

Conditions

Interventions

TypeNameDescription
DEVICEproduct: Innea Aqua vaginal useproduct object of the investigation: Innea Aqua for vaginal use, 2 mL product. Labelled as Innea Aqua.
DEVICEarm 2: standard of carethe comparator is the standard of care selected by the centre

Timeline

Start date
2025-09-25
Primary completion
2026-05-30
Completion
2026-06-30
First posted
2026-01-26
Last updated
2026-02-09

Locations

3 sites across 1 country: Romania

Source: ClinicalTrials.gov record NCT07367061. Inclusion in this directory is not an endorsement.

Clinical Investigation to Assess Safety and Efficacy of INNEA AQUA in Adult Women With Vulvo-Vaginal Atrophy (VVA) (NCT07367061) · Clinical Trials Directory