Early Laparoscopic Cholecystectomy Versus Percutaneous Cholecystostomy in Grade II Acute Cholecystitis Guidelines (PC)
Primary Purpose
Acute Cholecystitis, Empyema, Gallbladder
Status
Completed
Phase
Not Applicable
Locations
Egypt
Study Type
Interventional
Intervention
laparoscopic cholecystectomy
percutaneous cholecystostomy
Sponsored by
About this trial
This is an interventional treatment trial for Acute Cholecystitis focused on measuring moderate acute cholecystitis, percutaneous cholecystostomy
Eligibility Criteria
Inclusion Criteria:
- patients with one of the criteria stated by grade II (moderate) Tokyo guidelines for acute cholecystitis who were managed either by early LC or by a bridging PC followed by delayed LC.
Exclusion Criteria:
- grade I or III acute cholecystitis
- common bile duct stones or jaundice,
- Liver cirrhosis,
- severe upper abdominal adhesions,
- acalculous cholecystitis
- major comorbidities in which laparoscopic surgery is contraindicated.
- those who followed a conservative treatment for acute cholecystitis
Sites / Locations
- Alexandria university
- Faculty of Medicine
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Active Comparator
Arm Label
early laparoscopic cholecystectomy
percutaneous cholecystostomy
Arm Description
early laparoscopic cholecystectomy
percutaneous cholecystostomy first followed by delayed laparoscopic cholecystectomy
Outcomes
Primary Outcome Measures
operative difficulties as conversion, operative time, biliary injury
as assessed by the main surgeon
postoperative complications
as assessed by clavien dindo classification
Secondary Outcome Measures
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT04979936
Brief Title
Early Laparoscopic Cholecystectomy Versus Percutaneous Cholecystostomy in Grade II Acute Cholecystitis Guidelines
Acronym
PC
Official Title
Early Laparoscopic Cholecystectomy Versus Percutaneous Cholecystostomy Followed by Delayed Laparoscopic Cholecystectomy in Patients With Grade II Acute Cholecystitis According to Tokyo Guidelines
Study Type
Interventional
2. Study Status
Record Verification Date
July 2021
Overall Recruitment Status
Completed
Study Start Date
January 1, 2016 (Actual)
Primary Completion Date
January 31, 2021 (Actual)
Study Completion Date
January 31, 2021 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Alexandria University
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
The aim of this study is to compare between early laparoscopic cholecystectomy versus percutaneous cholecystostomy followed by delayed interval laparoscopic cholecystectomy as regards the operative and postoperative complications
Detailed Description
A-Study setting: Department of Surgery, main university hospital, Faculty of Medicine, Alexandria University, Egypt. The study was approved by the Ethics Committee of our institution.
B-Study design: Retrospective clinical trial C-Study subjects: The target population are patients with preoperative diagnosis of grade II acute cholecystitis Those patients were subjected to surgery either early laparoscopic cholecystectomy or delayed laparoscopic cholecystectomy after percutaneous cholecystostomy
Inclusion criteria of the study patients:
-Specific written informed consent approved by our Institution's Ethics Committee was obtained from all the treated patients.
Exclusion criteria:
-contraindication to laparoscopy,Refusal of study participation, cirrhosis, grade I or III acute cholecystitis D-Sample size calculation: a minimum sample size required per group is 88 to detect decline in the proportion of the primary outcome from 20% to 5%, at 5% level of significance and 80% power.
E-Sampling technique: By using eligibility criteria, 220 patients that were planned to undergo laparoscopic Cholecystectomy were randomly selected from the surgery department in main university hospital, Faculty of Medicine, Alexandria University. They were randomly separated into two groups:
An experiment group: (90 patients) underwent percutaneous cholecystostomy followed by delayed interval laparoscopic cholecystectomy A control group: (130 patients) underwent early laparoscopic cholecystectomy. All the participants were initially evaluated and re-evaluated during follow up period of 30 days for the outcome measures. Non blinded trial was done due to difficulty in using blinding in operative intervention.
Methods: every patient in the study sample was subjected to the followings:
History
Examination:
Investigations ( pre and postoperative):
Laboratory: WBC, CRP, lever functions Radiologic imaging: ultrasonography, CT abdomen
Intervention: An experiment group: underwent percutaneous cholecystostomy followed by delayed interval laparoscopic cholecystectomy.
A control group: underwent early laparoscopic cholecystectomy.
Surgical Technique: laparoscopic cholecysctomy Postoperative Course: post-operative complications
Outcome Measurement and Follow-Up
Follow up period: both groups were re-evaluated at 1, 2, 6 months. They were evaluated for the positive and negative outcome measures. There were no cases lost to follow up.
Outcome measures that were assessed after the follow up period were:
Primary outcome measures: operative and postoperative complications as conversion, biliary injury, bowel injury, they were assessed by clavien dindo classification
Secondary Outcome measures: ASA score, Tokyo score and some investigations.
Statistical analysis Statistical analysis was performed using the Statistical Package for the Social Sciences (SPSS) version 20 software (SPSS, Inc., Chicago, IL, USA). Quantitative variables were summarized using mean and standard deviation after data exploration using the Kolmogorov- Smirnov test. Qualitative variables were described using number and percent. Associations between the two groups and other categorical variables were assessed using Chi-square test (Fisher or Monte Carlo). Comparisons between the two groups as regards the quantitative variables were assessed using Student t-test. All Statistical tests were done at 5% level of Significance.
Risk estimates were calculated as Relative risk, Absolute risk reduction, Number needed to treat and population Attributable Risk percentage to detect the risk of development of the intraoperative and postoperative complications in the intervention and control group.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Acute Cholecystitis, Empyema, Gallbladder
Keywords
moderate acute cholecystitis, percutaneous cholecystostomy
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
220 (Actual)
8. Arms, Groups, and Interventions
Arm Title
early laparoscopic cholecystectomy
Arm Type
Active Comparator
Arm Description
early laparoscopic cholecystectomy
Arm Title
percutaneous cholecystostomy
Arm Type
Active Comparator
Arm Description
percutaneous cholecystostomy first followed by delayed laparoscopic cholecystectomy
Intervention Type
Procedure
Intervention Name(s)
laparoscopic cholecystectomy
Intervention Type
Procedure
Intervention Name(s)
percutaneous cholecystostomy
Primary Outcome Measure Information:
Title
operative difficulties as conversion, operative time, biliary injury
Description
as assessed by the main surgeon
Time Frame
at the time of cholecysctomy
Title
postoperative complications
Description
as assessed by clavien dindo classification
Time Frame
30 days after the operation
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
90 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
patients with one of the criteria stated by grade II (moderate) Tokyo guidelines for acute cholecystitis who were managed either by early LC or by a bridging PC followed by delayed LC.
Exclusion Criteria:
grade I or III acute cholecystitis
common bile duct stones or jaundice,
Liver cirrhosis,
severe upper abdominal adhesions,
acalculous cholecystitis
major comorbidities in which laparoscopic surgery is contraindicated.
those who followed a conservative treatment for acute cholecystitis
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
HANY MK EL-HADDAD, professor
Organizational Affiliation
alexandria university, faculty of medicine
Official's Role
Principal Investigator
Facility Information:
Facility Name
Alexandria university
City
Alexandria
Country
Egypt
Facility Name
Faculty of Medicine
City
Alexandria
Country
Egypt
12. IPD Sharing Statement
Plan to Share IPD
No
IPD Sharing Plan Description
data extracted from the hospital records. it is difficult to bring these data into public
Learn more about this trial
Early Laparoscopic Cholecystectomy Versus Percutaneous Cholecystostomy in Grade II Acute Cholecystitis Guidelines
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