Histological Analysis of Bellafill Injected Tissue at Various Time Points
NCT03327311 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 10
Last updated 2017-10-31
Summary
This is a prospective, in vivo proof-of-concept clinical study, where histopathologic examinations will be conducted at various timepoints following Bellafill injections.
Conditions
- Histopathology
Interventions
- DEVICE
-
Bellafill
Bellafill injected into site of pre-planned surgery (i.e., mini-abdominoplasty or redundant abdominal tissue removal) at two depths (dermis \& deep dermis).
Sponsors & Collaborators
-
Suneva Medical, Inc.
lead INDUSTRY
Principal Investigators
-
Nancy Seretta · Suneva Medical
Eligibility
- Min Age
- 21 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2015-08-31
- Primary Completion
- 2017-04-30
- Completion
- 2017-04-30
Countries
- United States
Study Locations
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