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Can Laparoscopic Cholecystectomy Difficulty Score Predict Difficult Surgery

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT04282759
Recruitment Status : Recruiting
First Posted : February 25, 2020
Last Update Posted : March 10, 2020
Sponsor:
Information provided by (Responsible Party):
Erguvan Nalıncıoğlu, Konya Training and Research Hospital

Brief Summary:

Laparoscopic cholecystectomy is the gold standard treatment method in symptomatic gallstone disease. However, complications that develop due to being a technical procedure tend to be more complex and more morbid—estimating how difficult the surgery will be before the operation will enable us to be more prepared both in terms of patient counseling and surgical team selection. Such a prediction will minimize the risk of complications and morbidity.

In our study, investigators used the scoring system "How to predict difficult laparoscopic cholecystectomy? Proposal for a simple preoperative scoring system?" which was published in "The American Journal of Surgery" in November 2016. Investigators wanted to evaluate prospectively adequate "Laparoscopic Cholecystectomy Difficulty Score," which was developed retrospectively, in determining the surgical difficulty preoperatively.


Condition or disease
Laparoscopic Cholecystectomy

Detailed Description:

ETHICAL BOARD APPROVAL

Konya Chamber of Commerce Education and Health Foundation was found ethically appropriate for the study according to the decision of Karatay University Ethical Board Presidency dated 18.06.2019 and numbered 2019/0051.

FEATURES OF THE STUDY AND SELECTION OF PATIENTS

Patients who were to be operated due to symptomatic cholelithiasis between 01.03.2020 and 31.07.2020 at the Health Sciences University (SBU) Konya Training and Research Hospital (KEAH) were included in the study. The study was done prospectively.

Laparoscopic Cholecystectomy Difficulty Score (DSLC) developed in the reference study will be used. The sex of the patients and whether they had an attack of cholecystitis will be recorded. Neutrophil count, fibrinogen, and ALP levels will be recorded from preoperatively routine blood tests. DSLC score will be calculated before the patient goes into surgery. How successful the scoring system is in determining the difficulty of the operation in the postoperative period will be analyzed statistically.

Thirteen surgeons will be included in the study. Based on the last ten surgery times, where each surgeon has no problems and has no technical difficulties, the average operation time will be calculated for each surgeon individually. In the reference study, it has been accepted that the surgeon's duration is more than 1.5 times or challenging to undergo open surgery. In our study, it will be considered as a difficult operation to exceed or exceed 1.5 times the surgeon's duration. Other than that, it will be considered a smooth operation. The biliary tract injuries that occurred in exposed cases will be classified according to the Strasberg classification. In the reference study, statistically significant score groups were formed as low risk of 0 points, medium risk of 1-4 points, high risk of 5-9 points, and a very high risk of 10 points. In our study, these score groups will be created, and statistical analysis will be made. Also, ROC (Reciever Operator Characteristics Curve) curve will be created with the scores obtained from the scoring system, and the specificity and sensitivity of the scoring system will be statistically put.

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Study Type : Observational
Estimated Enrollment : 1 participants
Observational Model: Case-Only
Time Perspective: Prospective
Official Title: Difficulty in Laparoscopic Cholecystectomy Score Can Determine the Operative Challenge.
Actual Study Start Date : March 1, 2020
Estimated Primary Completion Date : July 31, 2020
Estimated Study Completion Date : August 15, 2020



Primary Outcome Measures :
  1. Numerical recording of Difficulty Score of Laparoscopic Cholecystectomy (DSLC) [ Time Frame: The period of the study is between 1 March 2020 and 15 August 2020. ]
    Laparoscopic cholecystectomy scores of patients included in the study will be recorded. The relationship between the scoring system and the fact that the cases are easy or difficult will be analyzed statistically, in which predictive values determine the difficulty of the operation. The study will be terminated with the completion of the analysis.



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Ages Eligible for Study:   18 Years to 100 Years   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
The study population is comprised of patients between the ages of 18-100, who are referred to the general surgery clinic for laparoscopic cholecystectomy.
Criteria

Inclusion Criteria:

  • Patients who will be operated for biliary colic, chronic cholecystitis or symptomatic cholelithiasis,
  • Patients who have been treated with antibiotics before with the diagnosis of cholecystitis and have been planned for elective cholecystectomy,
  • Patients diagnosed with acute cholecystitis according to Tokyo criteria and cholecystectomy planned due to acute cholecystitis

Exclusion Criteria:

  • Patients under the age of 18,
  • Patients over 100 years old,
  • Patients diagnosed with choledocholithiasis with magnetic resonance cholangiopancreatography (MRCP),
  • Patients with cholangitis
  • Patients who have undergone endoscopic retrograde cholangiopancreatography (ERCP),
  • Patients who have undergone biliary system intervention before,
  • Patients scheduled for operation open cholecystectomy

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT04282759


Contacts
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Contact: Erguvan Nalincioglu, MD +905063191158 erguvannalincioglu@gmail.com
Contact: Alpaslan Sahin, MD +905052955095 drasahin@gmail.com

Locations
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Turkey
Konya Training and Research Hospital Recruiting
Konya, Turkey, 42090
Contact: Erguvan Nalincioglu, MD    +905063191158    erguvannalincioglu@gmail.com   
Sponsors and Collaborators
Konya Training and Research Hospital
Publications:
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Responsible Party: Erguvan Nalıncıoğlu, principal investigator, Konya Training and Research Hospital
ClinicalTrials.gov Identifier: NCT04282759    
Other Study ID Numbers: KonyaHPRC
First Posted: February 25, 2020    Key Record Dates
Last Update Posted: March 10, 2020
Last Verified: March 2020
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: Undecided

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No