Kerecis Case Registry for SurgiBind : Soft Tissue Reinforcement

Running, not enrolling

Conditions studied: Surgery-Complications

In brief

Registry Objectives The overall objective of the registry is to collect quality and safety data to assess the long-term outcomes of Kerecis Omega3 SurgiBind in surgical procedures to reinforce soft tissue and prevent surgical complications. The ultimate goal of the registry is to enhance the quality of care, patient outcomes and establish a resource to facilitate the use of fish skin in preventing surgical wound dehiscence and surgical site infection.

Key facts

Study ID

NCT05898711

Run by

Kerecis Ltd.

People needed

200

Starts

2022-01-27

Expected to finish

2026-01-27

Last updated by the study team

2024-12-31

Who can join

Age: 18 and older, up to 90. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Inclusion Criteria
• Age 18 and older
• Undergoing surgical procedure requiring soft tissue reinforcement with Kerecis Omega3 SurgiBind
• For example:
• Plastic reconstructive surgery
• Orthopedic surgery
• Cardiothoracic surgery
• Vascular Surgery
• General Surgery

You may not qualify if…

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• Participants who request not to be in the registry
• Life expectancy of less than 1 year

Where it is running

• Kerecis — Arlington, Virginia, United States

Full record on ClinicalTrials.gov

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