PerClot to Control Bleeding in Endoscopic Sinus Surgery

NCT02221128 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 12

Last updated 2014-10-03

No results posted yet for this study

Summary

A prospective, single centre, single arm study designed to collect clinical data on PerClot when used in subjects undergoing endoscopic sinus surgery.

Conditions

  • Sinusitis

Sponsors & Collaborators

  • CryoLife, Inc.

    collaborator INDUSTRY
  • CryoLife Europa

    lead INDUSTRY

Principal Investigators

  • David Roberts · Guy's and St Thomas' NHS Foundation Trust

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2014-07-31
Primary Completion
2014-09-30
Completion
2014-09-30

Countries

  • United Kingdom

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02221128 on ClinicalTrials.gov