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Clinical Trial Summary

The purpose of this study is to assess safety and performance with the use of the BiZact™ device in tonsillectomy procedures in children and adolescents.


Clinical Trial Description

A prospective, multi-center, single arm, study of BiZact™ on children and adolescents undergoing tonsillectomy.

Study Visits:

- Screening/Baseline

- Surgery, Day 0

- Post-Op Follow-up Day 1 - Day 7, Day 10, & Day 14 (Home assessments)

- Post-Op Follow-up Day 28 (Office Visit) ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03266094
Study type Interventional
Source Medtronic - MITG
Contact
Status Completed
Phase N/A
Start date September 30, 2018
Completion date July 11, 2019

See also
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