PerClot to Control Bleeding in Endoscopic Sinus Surgery

CryoLife

Status: Completed

Conditions: Sinusitis

Study type: Observational

Funder types: Industry

Identifiers

NCT02221128

PCT1402.001M(06/14)

Details and patient eligibility

About

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

Enrollment: 12 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Subjects having Endoscopic Sinus Surgery
• Subjects who will have PerClot used as a haemostatic agent
• Subjects willing and able to give consent
• Subjects over 18 years old

Exclusion criteria

• Subjects unable or unwilling to give consent for their data to be collected