Macrolane Retrospective Study

Galderma

Status: Completed

Conditions: Women Who Have Had Breast Enhancement With Macrolane VRF

Study type: Observational

Funder types: Industry

Identifiers

NCT01223963

31GB0902

Details and patient eligibility

About

This is a retrospective, multicenter chart review of medical records on the use of Macrolane for female breast enhancement.

The primary objective is to evaluate the safety profile of Macrolane Volume Restoration Factor 20 and Macrolane Volume Restoration Factor 30 when used for female breast enhancement in clinical practice.

Enrollment: 93 patients

Sex: Female

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Females treated with Macrolane Volume Restoration Factor 20 and/or Volume Restoration Factor 30 for breast enhancement.
• Signed Informed Consent

Exclusion criteria

• Subjects that have actively asked not to be contacted by the clinic
• Subjects that have participated or participates in clinical studies with Macrolane for breast enhancement

Trial design

93 participants in 1 patient group

Macrolane

Description:

Women that have had breast enhancement with Macrolane Volume Restoration Factor.