Clinical Trials Directory

Trials / Completed

CompletedNCT03068728

Analysis of Hemostatic Agents Compared to Physiologic Hemostasis

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
62 (actual)
Sponsor
St. Louis University · Academic / Other
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Not accepted

Summary

This study is a prospective comparison between absorbable hemostatic agents as a group and the body's natural hemostatic ability without aid of therapy in patients undergoing bilateral sinus surgery with or without septoplasty.

Detailed description

The purpose of this study is to evaluate the efficacy of absorbable hemostatic agents in comparison with physiologic hemostasis after endoscopic sinus surgery. The investigators aim to determine the relative efficacy of hemostatic agents to halt epistaxis and compare this with the degree of epistaxis observed without therapy and evaluate objective healing parameters.

Conditions

Interventions

TypeNameDescription
DEVICEArista
DEVICENexfoam
DEVICENasopore

Timeline

Start date
2014-05-13
Primary completion
2017-04-10
Completion
2017-04-10
First posted
2017-03-03
Last updated
2019-04-04

Source: ClinicalTrials.gov record NCT03068728. Inclusion in this directory is not an endorsement.