Status:
COMPLETED
Evaluation of Safety of HEMOBLAST Bellows in Spine Surgery
Lead Sponsor:
Dilon Technologies Inc.
Collaborating Sponsors:
Syneos Health
Conditions:
Surgical Bleeding
Eligibility:
All Genders
22+ years
Phase:
NA
Brief Summary
The purpose of this clinical investigation in open, elective, spine surgery is to collect data to support the removal of the neurosurgical exclusion from the currently approved indication for the use ...
Eligibility Criteria
Inclusion
- Subject is undergoing open, elective, spine surgery
- Subject or an authorized legal representative is willing and able to give prior written informed consent for investigation participation
- Subject is 22 years of age or older
- Subject does not have an active or suspected infection at the surgical site
- Subject in whom the Investigator is able to identify a Target Bleeding Site (TBS) for which any applicable conventional means for hemostasis are ineffective or impractical
- Subject has a TBS with a Surface Bleeding Severity Scale (SBSS) score of 1, 2, or 3
Exclusion
- Subject is undergoing an emergency surgical procedure
- Subject is undergoing a laparoscopic surgery
- Subject is undergoing a cervical spine surgery
- Subject is pregnant, planning on becoming pregnant during the follow-up period, or actively breast-feeding
- Subject has a platelet count \< 100,000 per microliter or International Normalized Ratio \> 1.5 within 4 weeks of surgery
- Subject receiving intravenous heparin within 12 hours before surgery or oral Coumadin within 2 days before surgery
- Subject receiving antiplatelet medications within 5 days prior to surgery
- Subject receiving aspirin within 7 days prior to surgery
- Subject has an active or suspected infection at the surgical site
- Subject has had or has planned to receive any organ transplantation
- Subject has a known sensitivity or allergy to bovine and/or porcine substance(s) or any other component(s) of the hemostatic agent
- Subject has a known sensitivity or allergy to Gadolinium
- The subject has a contra-indication for MRI or gadolinium contrast agent according to clinical guidelines, local regulations or manufacturer's recommendations
- Subject suffers from claustrophobia or fear of MRI, or has any contraindication to MRI (e.g., metal implants, spinal cord stimulator, etc. not suited to MRI)
- Subject has American Society of Anesthesiologists classification of \> 4
- Subject has a life expectancy of less than 3 months
- Subject has a documented severe congenital or acquired immunodeficiency
- Subject has religious or other objections to porcine, bovine, or human components
- Subject is currently participating or has participated in another clinical trial within the past 30 days and is receiving/has received an investigational drug, device, or biologic agent
- Per investigator opinion subject is unable to fully cooperate with the study protocol.
- The product will be placed in at the site where the dura is open
- The product will be placed in the intradural or cranial space
Key Trial Info
Start Date :
March 8 2021
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
February 5 2024
Estimated Enrollment :
60 Patients enrolled
Trial Details
Trial ID
NCT04734535
Start Date
March 8 2021
End Date
February 5 2024
Last Update
April 2 2024
Active Locations (5)
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1
University of Southern California
Los Angeles, California, United States, 900033
2
Indiana Spine Group
Carmel, Indiana, United States, 13225
3
Johns Hopkins Bayview Medical Center
Baltimore, Maryland, United States, 21224
4
Massachusetts General Hospital
Boston, Massachusetts, United States, 02114