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Seal-G Safety Study

NCT02825173 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 20

Last updated 2017-04-27

No results posted yet for this study

Summary

The purpose of this study is to farther assess the safety of the Seal-G Surgical Sealant for the reinforcement and protection of gastrointestinal anastomosis.

Conditions

  • Elective Surgical Procedures, Digestive System

Interventions

DEVICE

Seal-G

Intervention: Device: Seal-G Seal-G is applied adjunctively to cover standard closure techniques

Sponsors & Collaborators

  • Sealantis Ltd.

    lead INDUSTRY

Principal Investigators

  • Rina Lev, PhD · Sealantis Ltd.

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-08-31
Primary Completion
2016-11-30
Completion
2016-12-02

Countries

  • Israel
  • Italy

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02825173 on ClinicalTrials.gov