CompletedNot Applicable

a Flexible Wound Dressing for the Management of Genital Skin Conditions

Australia54 participantsStarted 2018-01-31

Plain-language summary

The objective of the study is to determine the efficacy of 7-0940 in the management of genital skin conditions in female patients

Who can participate

SexFEMALE

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Able to provide informed consent * Diagnosed genital skin condition Exclusion Criteria: * Unable to give informed consent * Patient unable to apply topical device * Allergy or intolerance to ingredients or excipients of the formulation of studied products

What they're measuring

gynaecological skin condition

Timeframe: Duration of the therapy will be according to physician's clinical practice. The average is 3 visits over a period of 3 to 6 months

Trial details

NCT IDNCT05396261

SponsorStratpharma AG

Sponsor typeINDUSTRY

Study typeINTERVENTIONAL

Primary completion2022-01-01

View on ClinicalTrials.gov More Vaginitis trials