Surgical Practices in Algeria : the Cholecystectomy

February 14, 2020 updated by: Anisse Tidjane, University of Oran 1

Surgical Practices During Cholecystectomy in Algeria: Results of a Survey

An anonymous national survey involving all practicing Algerian surgeons was conducted. At the end of the survey, all data were captured and processed using the SPSS v20 software; χ 2 tests were used to compare different groups of surgeons.

Study Overview

Detailed Description

An anonymous national survey involving all practicing Algerian surgeons was conducted, this survey started the 1st November 2016 and ended the 1st September 2017.

Any digestive , general and visceral surgeon practicing in Algeria was eligible for this survey, surgeons in training "residents" and Algerian surgeons exercising overseas was systematically excluded.

The aim was to analyse some practice in accordance with the recommendations of the Society of American Gastrointestinal and Endoscopic Surgeons who published a guideline in 2010.

This elaborated form was an electronic one; it was performed using the open electronic platform "Google Form", the conception of the form was made by A.Tidjane "surgeon" and he was the first participant to this survey, considering his participation he was excluded from the seizure of the data. The analysis and interpretation of data was made by S.Benilha "bio-statistician", B.Tabeti "surgeon" and A.Tidjane.

The form consisted of two parts, the first concerning the surgeon's Wilaya of exercise, the rank of health structure of practice, his professional position , and the year of his graduation , the second part concerning his practices during the performing CH and the questions concerned the use of laparoscopy or open surgery to perform CH, the number of Trocars used, the technique to access the peritoneal cavity, the surgical technique, the use of intraoperative cholangiography "IOC", the technique of extraction of the gallbladder, systematic gallbladder macroscopic and histological examination, the systematic abdominal cavity drainage, systematic use of postoperative antibiotic prophylaxis, and the optimal duration of postoperative stay in the case of optimal patient with no preoperative incident or postoperative complication. At the end of the survey a question was asked to surgeons about the occurrence during their professional practice of an operative bile duct injury.

The language of instruction of surgeons in Algeria is French; the French was used to draft this form. This electronic form was distributed by email to all surgeons in the authors Mail lists, those first contacted surgeons had the mission not only to participate in this survey but also had the mission of distributing the electronic form to their surgeon colleagues. All incomplete responses were excluded.

Statistical analyses:

At the end of the survey, all data were captured and processed using the SPSS v20 software (IBM Inc., Chicago, IL, USA), a χ 2 tests were used to compare some surgical practices in different groups of surgeons, a (P < 0.05) was considered statistically significant.

Study Type

Observational

Enrollment (Actual)

122

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 and older (ADULT, OLDER_ADULT)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

any surgeon practicing in Algeria is subject to this survey. THE surgeons in Algeria are holders of a "DEMS or equivalent" diploma which authorizes them to perform surgery in Algeria.

Description

Inclusion Criteria:

  • visceral an general surgeons practicing in Algeria.

Exclusion Criteria:

  • surgeon under training.
  • Algerian surgeon practicing abroad.

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
Influence of surgeons caracteristics on surgical practices
Time Frame: 11 months

The variables measured were of two types:

A - linked to the characteristics of the surgeon participating in the survey:

  • Exercice place.
  • Type of exercise structure.
  • Grade of surgeon.
  • Date of graduation.
  • Weekly volume of surgery.
  • Use of laparoscopic surgery.

B- Related to the surgeon's own practices when he performs this surgery:

  • Laparoscopic or open cholecystectomy.
  • Respect for the different dissection times.
  • Number of trocars.
  • Number of clips placed for the cystic duct and the cystic artery.
  • Rule of extraction of the gallbladder.
  • Use of antibiotics postoperatively.
  • Abdominal drainage.
  • length of hospital stay after surgery.

To find a correlation between the variables of Group A and B, a test, a χ 2 tests were used to compare some surgical practices in different groups of surgeons, a (P < 0.05) was considered statistically significant.

11 months

Collaborators and Investigators

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

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 (ACTUAL)

November 1, 2016

Primary Completion (ACTUAL)

September 1, 2017

Study Completion (ACTUAL)

September 1, 2017

Study Registration Dates

First Submitted

February 12, 2020

First Submitted That Met QC Criteria

February 12, 2020

First Posted (ACTUAL)

February 17, 2020

Study Record Updates

Last Update Posted (ACTUAL)

February 18, 2020

Last Update Submitted That Met QC Criteria

February 14, 2020

Last Verified

February 1, 2020

More Information

Terms related to this study

Other Study ID Numbers

  • UOran1

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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