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N/A
25 Years
50 Years
Open (Enrolling)
Female
Breast Enhancement

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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:

  • Breast Enhancement

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