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A Trial Comparing Wound Drainage and Post-operative Complications With and Without the Use of EVICEL™ Fibrin Sealant in Thyroidectomy

Goiter Clinical Trial

Official title:
A Randomized, Double-Blind, Placebo-Controlled Trial Comparing Wound Drainage and Post-operative Complications With and Without the Use of EVICEL™ Fibrin Sealant in Thyroidectomy

Clinical Trial Summary

Primary Objectives

- To compare the amount of post-operative wound drainage between the group of patients in which EVICEL™ spray is utilized (Arm A), and the group of patients in which an EVICEL™ placebo is utilized (Arm B).

- To compare the length of time to drain removal between Arm A and Arm B. Secondary objectives

- To compare the incident or rates of seroma, hematoma, and post-operative edema between the two groups.

- To compare the reported pain experienced in each group at selected time points using a standard numerical rating scale (NRS).

- To compare the length of hospital stay between the two groups of patients.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01226914
Study type Interventional
Source Medical University of South Carolina
Contact
Status Completed
Phase N/A
Start date June 2010
Completion date July 2014
View Details
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