GATT-Patch Versus SURGICEL® Original in Minimally Invasive Liver and Gallbladder Surgery

Launched by GATT TECHNOLOGIES BV · Jun 9, 2023

Keywords

ClinConnect Summary

This clinical trial is looking at two different products—GATT-Patch and SURGICEL® Original—to see which one works better for controlling mild to moderate bleeding during minimally invasive surgeries for the liver and gallbladder. If you or a family member are planning to have elective surgery on the liver, such as gallbladder removal, and are at least 22 years old, you might be eligible to participate. The study is open to both men and women, and participants will need to agree to take part by signing a consent form.

If you join the study, you will be randomly assigned to receive either GATT-Patch or SURGICEL® Original during your surgery. Both products are used to help stop bleeding when traditional methods like stitches or cauterization aren’t effective. The trial is being conducted at multiple centers, and your doctor will explain everything you need to know about the trial, including potential risks and benefits, before you decide to participate. It's important to note that there are specific health criteria that might exclude you from the trial, such as certain medical conditions or taking specific medications.

Gender

ALL

Eligibility criteria

• Inclusion Criteria:
• • Subject is scheduled to undergo elective minimally invasive (robotic or laparoscopic) surgery on the liver, including cholecystectomy
• • Subject is willing and able to give written informed consent for the clinical investigation participation
• • Subjects is 22 years of age or older at the time of enrollment; and
• • Subject has been informed of the nature of the clinical investigation.
• A subject must meet all of the following intra-operative inclusion criteria to be enrolled into the clinical investigation:
• • Subject undergoes a fully minimally invasive surgical approach without the use of a hand port at the time of randomization and application of the patch;
• • Subject in whom the Investigator is able to identify a target bleeding site at the liver resection plane for which any applicable conventional means for hemostasis (e.g. suture, ligature or cautery) are ineffective or impractical, and the choice is made to use a hemostatic agent to stop the bleeding
• • Pressure on the surface of the hemostatic agent can be applied with the minimally invasive instruments to achieve hemostasis
• • Subject has a target bleeding site with a SBSS of 1, 2, or 3 (e.g. reflecting minimal, mild or moderate bleeding severities)
• Exclusion Criteria:
• • The target bleeding site is from a large defect in an artery or vein that requires vascular reconstruction with maintenance of vessel patency
• • Subject is scheduled to undergo surgery on organs other than the liver and its associated biliary and vascular system
• • Subject is scheduled to undergo a staged liver surgery procedure (e.g., Associating Liver Partition and Portal vein ligation for Staged hepatectomy \[ALPPS\])
• • Subject is taking multiple antithrombotic therapies in therapeutic dosage up to the time of surgery, but allowing exclusive use of acetylsalicylic acid
• • Subject has platelet count \<100 x 109/L, an activated partial thrombin time of \>100s, or international normalized ratio \>2.5
• • Subject has a total bilirubin level of ≥2.5 mg/dl
• • Subject is pregnant, planning on becoming pregnant or actively breastfeeding during the 3-month follow-up period
• • Subject has a known hypersensitivity to brilliant blue (FD\&C Blue #1), porcine gelatin
• • Subject who has religious objections to receiving products containing porcine
• • Subject has an active or suspected infection at the bleeding site
• • Subject in whom the investigational device will be used at the site of a synthetic graft or patch implant
• • Subject has a life expectancy of less than 3 months
• • Subject has a documented severe congenital or acquired immunodeficiency
• • Subject has had or has planned to receive any organ transplantation
• • Subject undergoes surgery with the indication of being a living liver donor
• • Subject is currently participating or has participated in another clinical investigation within the past 30 days that may affect the endpoints of the study, such as trials related to the surgical procedure and anti-coagulation
• • Subject is not appropriate for inclusion in the clinical investigation, per the medical opinion of the Investigator
• • Subject has any incidental (pre- and peri-operative) findings deemed by the Investigator to potentially jeopardize the safety or welfare of the subject