Actively Recruiting
Use of Stratafix Symmetric™ to Prevent Incisional Hernia in Gastrointestinal and Abdominal Surgery
Led by West Michigan Cancer Center · Updated on 2024-02-02
100
Participants Needed
1
Research Sites
156 weeks
Total Duration
On this page
Sponsors
W
West Michigan Cancer Center
Lead Sponsor
E
Ethicon, Inc.
Collaborating Sponsor
AI-Summary
What this Trial Is About
Comparing the use of Stratafix Symmetric™ sutures to standard laparotomy closure sutures.
CONDITIONS
Official Title
Use of Stratafix Symmetric™ to Prevent Incisional Hernia in Gastrointestinal and Abdominal Surgery
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Participant is a male or female 18 years of age or older.
- Participant is a current patient at West Michigan Cancer Center.
- Participant is undergoing liver, pancreas or biliary or gastrointestinal surgery of a combination of the above, or other major oncological surgery.
- Participant is willing and able to provide written informed consent before surgery.
You will not qualify if you...
- Participant has hemodynamic instability at the conclusion of the surgery.
- Participant has history of previous ventral incisional hernia.
- Participant has a mental condition rendering the subject incapable of understanding the nature, scope and consequences of the study.
AI-Screening
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Trial Site Locations
Total: 1 location
1
West Michigan Cancer Center
Kalamazoo, Michigan, United States, 49007
Actively Recruiting
Research Team
W
Wendi Mitchell
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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