Trial Information
Inclusion Criteria:
- subject treated with NASHA-gel in the breasts in study 31GB0607
- signed informed consent
Exclusion Criteria:
- no exclusion criteria in this study
Type of Study:
Observational
Study Design:
Time Perspective: Prospective
Outcome Measure:
Evaluate if study product has been completely degraded in the breast 4 years post treatment in study 31GB0607, using MRI
Outcome Time Frame:
4 years
Safety Issue:
Yes
Principal Investigator
Per Hedén, M.D.
Investigator Role:
Principal Investigator
Investigator Affiliation:
Akademikliniken, Stockholm, Sweden
Authority:
Sweden: Regional Ethical Review Board
Study ID:
31GB1103
NCT ID:
NCT01609400
Start Date:
December 2011
Completion Date:
May 2014
Related Keywords: