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Spots Global Cancer Trial Database for Efficacy and Safety of LifeSeal™ Kit for Colorectal Staple Line Sealing

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Trial Identification

Brief Title: Efficacy and Safety of LifeSeal™ Kit for Colorectal Staple Line Sealing

Official Title: Efficacy and Safety of LifeSeal™ Kit for Staple Line Sealing in Colorectal and Coloanal Anastomoses: A Prospective Randomized Study

Study ID: NCT02907385

Interventions

LifeSeal™ Kit

Study Description

Brief Summary: LifeSeal™ Kit, surgical sealant designed for staple-line reinforcement that is applied over the anastomotic line to prevent bowel content leakage until full physiological function is restored. RATIONALE : Postoperative anastomotic leakage is one of the most devastating and feared complications in colorectal surgery. The risk of postoperative anastomotic leakage varies widely depending on the level of anastomosis while the risk is higher in low anastomosis. In order to best demonstrate the benefits of LifeSeal™ in providing staple line reinforcement and helping to reduce leaks, the study includes high risk anastomoses, defined as colorectal and coloanal anastomoses performed within 10 cm from the anal verge. STUDY DESIGN: This study is designed as a prospective, multi-center, multinational randomized, single-blind, double armed study PRIMARY OBJECTIVE: The primary objective of this study is to assess the efficacy and safety of LifeSeal™ Kit as measured by the change in overall anastomotic leak rates in subjects undergoing low anterior resection with an anastomosis below 10 cm from the anal verge, over the first 17 weeks after surgery. SECONDARY OBJECTIVES: The secondary objective of this study is to assess the incidence of post-operative leaks and additional benefits that could be related to the use of LifeSeal™ Kit such as reducing the severity and improving the outcome of a leak once it has occurred. In addition, the study will allow for collection and analysis of additional safety data and usability assessment of the device, medical resource utilization, and health related quality of life measures.

Detailed Description:

Eligibility

Minimum Age: 21 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

University of Southern CA, Los Angeles, California, United States

Stanford University, Stanford, California, United States

Florida Hospital, Florida City, Florida, United States

Tampa General Hospital, Tampa, Florida, United States

Cleveland Clinic Florida, Weston, Florida, United States

University of Chicago, Chicago, Illinois, United States

Franciscan, Indianapolis, Indiana, United States

Indiana University, Indianapolis, Indiana, United States

Ochsner Clinic Foundation, Jefferson, Louisiana, United States

Johns Hopkins Hospital, Baltimore, Maryland, United States

Medical University SC (MUSC), Worcester, Massachusetts, United States

University of Massachusetts, Worcester, Massachusetts, United States

Spectrum Health, Grand Rapids, Michigan, United States

Washington University, Saint Louis, Missouri, United States

Albany medical center, Albany, New York, United States

New York University, New York, New York, United States

Cleveland Clinic, Cleveland, Ohio, United States

University Hospital Cleveland Medical Center, Cleveland, Ohio, United States

Penn state university, State College, Pennsylvania, United States

Duke University, Durham, South Carolina, United States

University of Vermont, Burlington, Vermont, United States

University of Virginia, Charlottesville, Virginia, United States

Medical College of Wisconsin, Milwaukee, Wisconsin, United States

OLV Ziekenhuis Aalst, Aalst, , Belgium

Ziekenhuis Oost-Limburg, Genk, , Belgium

Gent University Hospital, Gent, , Belgium

University Hospital Leuven, Leuven, , Belgium

Bispebjerg Hospital, Copenhagen, , Denmark

Zealand University Hospital, Roskilde, , Denmark

Beilinson Rabin Medical Center, Petah Tikva, , Israel

Sourasky Medical Center, Tel Aviv, , Israel

Assaf Harofeh Medical Center, Tzrifin, , Israel

Policlinico S.Orsola Malpighi, Bologna, , Italy

Humanitas Research Hospital, Milano, , Italy

University of Padova, Padova, , Italy

Catharina Hospital Eindhoven, Eindhoven, , Netherlands

Lund University Hospital, Malmö, , Sweden

Karolinska University Hospital, Stockholm, , Sweden

Uppsala University Hospital, Uppsala, , Sweden

Contact Details

Useful links and downloads for this trial

Clinicaltrials.gov

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