A Clinical Study Comparing Standard Anastomosis Closure Technique to Standard Closure Techniques Plus Sylys® Surgical Sealant

ClinicalTrials.gov ID: NCT02841891

Public ClinicalTrials.gov record NCT02841891. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

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ClinicalTrials.gov public records Last synced Oct 20, 2026, 3:58 PM EDT

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Official title

A Prospective, Randomized, Controlled, Multicenter Clinical Study Comparing Standard Anastomosis Closure Technique to Standard Closure Techniques Plus Sylys® Surgical Sealant

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The Cohera Sylys® Surgical Sealant study is a prospective, randomized, controlled, multicenter clinical study comparing standard anastomosis closure technique (Control) to standard closure technique plus Sylys® Surgical Sealant (Test) in patients undergoing a colectomy procedure with a stapled anastomosis.

Study identification

NCT ID: NCT02841891
Recruitment status: Terminated
Study type: Interventional
Phase: Not applicable
Lead sponsor: Cohera Medical, Inc.; Industry
Enrollment: 58 participants

Conditions and interventions

Conditions

Interventions

Sylys® Surgical Sealant Device
Stapled Anastomosis Colectomy Procedure Procedure

Device · Procedure

Eligibility (public fields only)

Age range: 22 Years and older
Sex: All
Healthy volunteers: Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date: Jul 2016 (Type not available)
Primary completion: Aug 13, 2018 (Actual)
Completion: Aug 13, 2018 (Actual)
Last update posted: Aug 16, 2018

2016 – 2018

United States locations

U.S. sites: 16
U.S. states: 11
U.S. cities: 15

Facility	City	State	ZIP	Site status
University of Alabama at Birmingham	Birmingham	Alabama	35294	—
University of Southern Alabama	Mobile	Alabama	36617	—
University of California Irvine	Orange	California	92868	—
University of Colorado Denver	Denver	Colorado	80204	—
Mayo Clinic Florida	Jacksonville	Florida	32224	—
University of South Florida	Tampa	Florida	33606	—
Tulane	New Orleans	Louisiana	70112	—
Ochsner Medical Center	New Orleans	Louisiana	70121	—
Mayo Clinic Rochester	Rochester	Minnesota	55905	—
Stony Brook University Hospital	Stony Brook	New York	11794	—
Duke University	Durham	North Carolina	27710	—
Medical University of South Carolina	Charleston	South Carolina	29425	—
Baylor Scott & White Research Institute	Dallas	Texas	75246	—
Houston Methodist	Houston	Texas	77030	—
Intermountain Healthcare	Ogden	Utah	84403	—
Univeristy of Utah	Salt Lake City	Utah	84132	—

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows: Public field values for ClinicalTrials.gov record NCT02841891, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do: No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from: Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh: Last update posted Aug 16, 2018 · Synced Oct 20, 2026

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The complete public registry record, listed eligibility criteria, and available contact information for NCT02841891 live on ClinicalTrials.gov.

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