LifeSeal™ Preliminary Study in Subjects Undergoing Low Anterior Resection

NCT01790230 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 10

Last updated 2013-09-04

No results posted yet for this study

Summary

A preliminary Study in Subjects Undergoing Low Anterior Resection

Conditions

Interventions

DEVICE

LifeSeal™ Kit

Application of LifeSeal™ Kit for staple line reinforcement during open GI surgeries in Low Anterior Resection

Sponsors & Collaborators

  • LifeBond Ltd.

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-01-31
Primary Completion
2013-08-31
Completion
2013-08-31

Countries

  • Sweden

Study Locations

More Related Trials

Entities

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 NCT01790230 on ClinicalTrials.gov