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Extended Antibiotic Therapy in Postoperative of Laparoscopic Cholecystectomy in Acute Cholecystitis

Primary Purpose

Acute Cholecystitis

Status
Completed
Phase
Phase 4
Locations
Argentina
Study Type
Interventional
Intervention
Amoxicillin clavulanic
Placebo
Sponsored by
Hospital Italiano de Buenos Aires
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Acute Cholecystitis focused on measuring Acute cholecystitis., Amoxicillin clavulanic

Eligibility Criteria

18 Years - 85 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • 18 to 85 years old
  • Patients with diagnose of mild or moderate acute cholecystitis.
  • Underwent laparoscopic cholecystectomy on Italian Hospital of Buenos Aires

Exclusion Criteria:

  • They refuse to participate from the trial or the process of informed consent.
  • Have known allergies or hypersensitivity to Mosapride or lactose (used for placebo).
  • Patients with severe cholecystitis
  • Patients with moderate cholecystitis who presents liver abscess, gallbladder abscess, cholangitis or bile peritonitis.
  • Intraoperative findings like liver cancer, liver metastases, common bile duct stones or gallbladder carcinoma.
  • Patients with conversion to laparotomy
  • Previous treatment with antibiotics for more than five days.
  • Patients with active oncological diseases, AIDS, diabetes, transplanted.

Sites / Locations

  • Hospital Italiano de Buenos Aires

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

Group A (Amoxicillin Clavulanic)

Placebo

Arm Description

Intake of active drug (Amoxicillin Clavulanic). 3 g per day divided into 3 oral intakes of 1 g each (2 pill of Amoxicillin Clavulanic every 8 hrs). This treatment will begin on postoperative day 1 for 5 days.

Intake of placebo (Lactose). 1 pill of the same characteristics as Amoxicillin clavulanic every 8 hs. This will begin on postoperative day 1 for 5 days.

Outcomes

Primary Outcome Measures

Incidence of infectious postoperative complications
Incidence of infectious postoperative complications in patients who underwent a laparoscopic cholecystectomy due to acute mild and moderate cholecystitis, with antibiotics or placebo

Secondary Outcome Measures

Number of days of hospital stay or readmissions.
To evaluate hospital stay.
Number of surgical reinterventions or reoperations.

Full Information

First Posted
February 5, 2014
Last Updated
February 25, 2019
Sponsor
Hospital Italiano de Buenos Aires
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1. Study Identification

Unique Protocol Identification Number
NCT02057679
Brief Title
Extended Antibiotic Therapy in Postoperative of Laparoscopic Cholecystectomy in Acute Cholecystitis
Official Title
Extended Antibiotic Therapy in Postoperative of Laparoscopic Cholecystectomy Due to Acute Cholecystitis. Is it Necessary?
Study Type
Interventional

2. Study Status

Record Verification Date
February 2019
Overall Recruitment Status
Completed
Study Start Date
February 2014 (undefined)
Primary Completion Date
March 2017 (Actual)
Study Completion Date
May 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Hospital Italiano de Buenos Aires

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Acute cholecystitis (AC) is a very common complication of cholelithiasis, encountered in 20% of symptomatic patients. Nowadays laparoscopic cholecystectomy (LC) is the standard treatment in mild and moderates forms of diseases and antibiotic therapy in the postoperatory of these patients remains under discussion. However in the beginning, AC presents itself as an steril process, the obstruction of the cystic duct initiates a cascade of inflammation, ischaemia and necrosis, as well as bacterial proliferation within the gallbladder lumen. Bactibilia was a significant factor associated with total, as well as infectious, operative complications. Regarding this, for some authors, monotherapy with amoxicillin clavulanic (AMC) would be the best treatment after LC in patients with mild and moderate cholecystitis without intraoperative complications such as bile peritonitis, cholangitis, gallbladder perforation or abscess. In the other hand, others do not prescribe antimicrobial treatment after surgery in these selected patients. There is controversy regarding the postoperative treatment with antibiotics in patients with mild and moderate cholecystitis and all the evidence about this topic. Therefore, investigators decided to conduct a prospective randomized study in patients undergoing laparoscopic cholecystectomy for acute mild and moderate cholecystitis cancer. The patients will be randomized to receive AMC or placebo after surgery. With this study investigators intend to prove that are no clinical differences in postoperative outcomes between patients treated with AMC and placebo. The primary aim of the trial is to assess that there are no benefits in the use of postoperative antibiotics in patients whit mild or moderate acute cholecystitis in whom a laparoscopic cholecystectomy was performed.
Detailed Description
Double blind randomized clinical trial

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Acute Cholecystitis
Keywords
Acute cholecystitis., Amoxicillin clavulanic

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
Care ProviderInvestigator
Allocation
Randomized
Enrollment
200 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Group A (Amoxicillin Clavulanic)
Arm Type
Active Comparator
Arm Description
Intake of active drug (Amoxicillin Clavulanic). 3 g per day divided into 3 oral intakes of 1 g each (2 pill of Amoxicillin Clavulanic every 8 hrs). This treatment will begin on postoperative day 1 for 5 days.
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Intake of placebo (Lactose). 1 pill of the same characteristics as Amoxicillin clavulanic every 8 hs. This will begin on postoperative day 1 for 5 days.
Intervention Type
Drug
Intervention Name(s)
Amoxicillin clavulanic
Other Intervention Name(s)
Optamox
Intervention Description
3 g per day divided into 3 oral intakes of 1 g each (2 pill of Amoxicillin Clavulanic every 8 hrs). This treatment will begin on postoperative day 1 for 5 days.
Intervention Type
Drug
Intervention Name(s)
Placebo
Other Intervention Name(s)
Lactose
Intervention Description
1 pill of the same characteristics as Amoxicillin clavulanic every 8 hs. This will begin on postoperative day 1 for 5 days.
Primary Outcome Measure Information:
Title
Incidence of infectious postoperative complications
Description
Incidence of infectious postoperative complications in patients who underwent a laparoscopic cholecystectomy due to acute mild and moderate cholecystitis, with antibiotics or placebo
Time Frame
30 days
Secondary Outcome Measure Information:
Title
Number of days of hospital stay or readmissions.
Description
To evaluate hospital stay.
Time Frame
30 days
Title
Number of surgical reinterventions or reoperations.
Time Frame
30 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 18 to 85 years old Patients with diagnose of mild or moderate acute cholecystitis. Underwent laparoscopic cholecystectomy on Italian Hospital of Buenos Aires Exclusion Criteria: They refuse to participate from the trial or the process of informed consent. Have known allergies or hypersensitivity to Mosapride or lactose (used for placebo). Patients with severe cholecystitis Patients with moderate cholecystitis who presents liver abscess, gallbladder abscess, cholangitis or bile peritonitis. Intraoperative findings like liver cancer, liver metastases, common bile duct stones or gallbladder carcinoma. Patients with conversion to laparotomy Previous treatment with antibiotics for more than five days. Patients with active oncological diseases, AIDS, diabetes, transplanted.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Martin de Santibañes, MD
Organizational Affiliation
Hospital Italiano de Buenos Aires
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Diego Giunta, MD
Organizational Affiliation
Hospital Italiano de Buenos Aires
Official's Role
Study Director
Facility Information:
Facility Name
Hospital Italiano de Buenos Aires
City
Capital Federal
State/Province
Buenos Aires
ZIP/Postal Code
1199
Country
Argentina

12. IPD Sharing Statement

Citations:
PubMed Identifier
18579815
Citation
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Results Reference
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Results Reference
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PubMed Identifier
19621660
Citation
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PubMed Identifier
3558716
Citation
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PubMed Identifier
19638912
Citation
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Results Reference
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PubMed Identifier
22872303
Citation
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Extended Antibiotic Therapy in Postoperative of Laparoscopic Cholecystectomy in Acute Cholecystitis

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