Standarization for Stappler Application During Sleeve Gastrectomy (LSG)

March 28, 2016 updated by: Sergio Gabriel Susmallian, Assuta Medical Center

Implication and Factors Influencing the Decision to Select Srapplers During Laparoscopic Sleeve Gastrectomy.

Sleev gastrectomy is a procedure performed for permanent treatment of obesity. For the procedure, cutting of the stomach is performed with differents long of stapplers.

The aim of the study is to determine wich long of stappler is applicable in any stage of the procedure ans the variation expected.

Study Overview

Status

Completed

Conditions

Obesity

Detailed Description

After permormed laparoscopic sleeve gastrectomy the stonach retrieved for pathology study will be messured in three ponts: antrum, body and fundus.

In each point medition of the two walls and any wall (anterior and posterior) will be messurd.

Those data will be stariscally analized to perform a applicable guidelines for stapller selection.

Study Type

Observational

Enrollment (Actual)

100

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

Israel
- - Tel Aviv, Israel
    - Assuta MC

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 70 years (Adult, Older Adult)

Accepts Healthy Volunteers

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

patients underwnt laparoscopic sleev gastrectomy between 18 y.o. and 70 y.o.

Description

Inclusion Criteria:

every laparoscopic sleeve gastrectomy
between 18 y.o. and 70 y.o.
no previous gastric operation

Exclusion Criteria:

under 18 y.o. or over 70 y.o. previous gastric surgery

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
differences in wall mesurments Time Frame: 3 month	during 3 month the data will be collected and proceceed	3 month

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Assuta Medical Center

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

May 1, 2014

Primary Completion (Actual)

September 1, 2015

Study Completion (Actual)

September 1, 2015

Study Registration Dates

First Submitted

February 19, 2014

First Submitted That Met QC Criteria