A Study of BiZact™ on Adults Undergoing Tonsillectomy

Status Completed

Clinical Trial Summary

The purpose of this study is to assess the severity of post-operative pain following the use of the BiZact™ device in adult (≥22 years of age in United States and ≥18 years of age in Europe) tonsillectomy procedures.

Clinical Trial Description

Study Design: Prospective, multi-center, single-arm non-comparative pilot study to assess the severity of post-operative pain with the use of BiZact™ for tonsillectomy.

Study Visits:

- Screening

- Surgery, Day 0

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

- Post-Op Follow-up Day 14 (Office Visit) ;

Study Design

Related Conditions & MeSH terms

Tonsillectomy

Clinical Trial Details

NCT number	NCT02876575
Study type	Interventional
Source	Medtronic - MITG
Contact
Status	Completed
Phase	N/A
Start date	February 13, 2017
Completion date	October 24, 2018

View Details

See also
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