Clinical Investigation To Evaluate Cerviron Ovules® in Symptomatic Vaginitis

Inclusion Criteria: * Adult females, aged 18 years to 65 years; * Subjects presenting two or more vaginal symptoms such as leucorrhoea, pruritus, burning sensation, erythema, pain, odour, dysuria, or dyspareunia; * Subjects with a diagnosis of either non-infectious vaginitis, or endogenous, symptomatic infection; * Negative for Gardnerella vaginalis, Candida albicans, Trichomonas vaginalis; * Subjects willing to provide signed informed consent to clinical investigation participation. Exclusion Criteria: * Subjects in menstrual period or suffering from menorrhagia; * Colpectomy; * Subjects with undiagnosed abnormal genital bleeding; * Subject with vulvar, vaginal or cervical cancer; * Known, active sexually transmitted infection (STI) in partner, as per anamnesis; * Subjects with HIV or other immunodeficiency; * Subjects with any pathology of the female reproductive organs; * Known allergy or hypersensitivity to the medical device ingredients; * Use of spermicides; * Use of diaphragm; * Concomitant topical or systemic anti-infective treatment; * Unable to comply with visit procedures; * Subjects included in other clinical investigations;