Status:

TERMINATED

Post-Market Evaluation of HEMOBLAST™ Bellows in Open Gynecological, Urological, ENT, Head, Neck, and Vascular Surgeries

Lead Sponsor:

Biom'Up France SAS

Conditions:

Hemostasis

Eligibility:

All Genders

18+ years

Brief Summary

A prospective, multi-center, multi-national single arm study to evaluate the performance and safety of HEMOBLAST™ Bellows in open gynecological, urological, ENT and head and neck, and vascular surgery...

Detailed Description

A prospective, multi-center, multi-national single arm study conducted in Austria, France, and Germany to evaluate the performance and safety of HEMOBLAST™ Bellows in open gynecological, urological, E...

Eligibility Criteria

Inclusion

  • Pre-operative
  • Patient is undergoing a non-emergent open gynecological, urological, ENT, head and neck, or vascular surgery
  • Patient is willing and able to give prior written informed consent for investigation participation;
  • Patient is 18 years of age or older.
  • Intra-operative Inclusion Criteria
  • Patient has one or more target bleeding sites (TBS) for which control of bleeding by conventional procedures is ineffective or impractical.
  • The TBS(s) has been treated with HEMOBLASTTM Bellows as per their instructions for use.

Exclusion

  • Patient is pregnant, planning on becoming pregnant during the follow-up period, or actively breast-feeding;
  • Patient has a known sensitivity or allergy to bovine and/or porcine substance(s) or any other component(s) of the hemostatic agent;
  • Patient has religious or other objections to porcine, bovine, or human components;
  • Patient has any significant coagulation disorder;
  • Patient has any other contraindications, warnings, precautions of the Approved Instruction For Use of HEMOBLAST™ Bellows preventing his/ her inclusion
  • Patient is not appropriate for inclusion in the clinical trial, per the medical opinion of the Investigator

Key Trial Info

Start Date :

May 9 2019

Trial Type :

OBSERVATIONAL

Allocation :

ACTUAL

End Date :

July 27 2021

Estimated Enrollment :

64 Patients enrolled

Trial Details

Trial ID

NCT03873168

Start Date

May 9 2019

End Date

July 27 2021

Last Update

August 30 2021

Active Locations (9)

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Page 1 of 3 (9 locations)

1

Uniklinikum

Salzburg, Austria

2

Centre Hospitalier Universitaire d'Angers

Angers, France

3

CHU Grenoble

Grenoble, France

4

Hopital Saint-Joseph

Paris, France, 75014