Registry Study for the Use of HEMOBLAST™ Bellows in Abdominoplasty
Withdrawn before enrolling
Conditions studied: Abdominoplasty
In brief
The purpose of this post-market observational registry is to collect additional data on the safety and efficacy of the HEMOBLAST™ Bellows device in abdominoplasty procedures.
Key facts
- Study ID
- NCT03770195
- Run by
- Biom'Up France SAS
- People needed
- 0
- Starts
- 2018-11-13
- Expected to finish
- 2018-12-12
- Last updated by the study team
- 2018-12-14
Who can join
Age: any. Sex: any. Healthy volunteers: not accepted.
Where it is running
- Hunstad Kortesis Bharti Cosmetic Surgery — Huntsville, North Carolina, United States
Full record on ClinicalTrials.gov
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