Macrolane Prospective Survey

A Multi-center, Non-interventional, Prospective Study to Monitor Long Term Safety in Female Subjects After Treatment With Macrolane Volume Restoration Factor 20 and/or Macrolane Volume Restoration Factor 30 in the Breasts.

Status

Withdrawn

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT01223066

Enrollment

Registered

2010-10-18

Start date

2010-09-30

Completion date

2010-10-31

Last updated

2022-08-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Females Recently Treated With Macrolane VRF in the Breasts

Keywords

Macrolane

Brief summary

The study objective is to evaluate the long term safety when Macrolane Volume Restoration Factor is used in female breasts in clinical practice.

Interventions

None listed

Study design

Observational model

COHORT

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

FEMALE

Healthy volunteers

Yes

Inclusion criteria

* Females recently treated with Macrolane Volume Restoration Factor in the breasts. * Signed informed consent

Exclusion criteria

* There are no

Design outcomes

Primary

Measure	Time frame
Adverse events	up to 5 years

Countries

Sweden

Outcome results