|
Home
Search
Study Topics
Glossary
|
![]() |
![]() |
|
![]() |
|
![]() |
|
![]() |
![]() |
![]() |
|
![]() |
![]() |
||||||||||||||||||||||||||||||||||||
| Sponsor: | Hadassah Medical Organization |
|---|---|
| Information provided by: | Hadassah Medical Organization |
| ClinicalTrials.gov Identifier: | NCT00557453 |
Purpose
The treatment of acute cholecystitis includes limited oral intake, antibiotics and early or delayed surgery. To date there are no randomized trials proving the benefit of antibiotic treatment.
The aim of this study is to prospectively and randomly compare between patients that are admitted for acute cholecystitis and treated with or without antibiotics.
| Condition | Intervention |
|---|---|
|
Acute Cholecystitits |
Drug: Antibiotic treatment Drug: No antibiotics |
| Study Type: | Observational |
| Study Design: | Case Control, Prospective |
| Official Title: | The Role of Antibiotic Treatment in Patients With Acute Mild Cholecystitis - A Prospective Randomized Controlled Trial |
| Estimated Enrollment: | 120 |
| Study Start Date: | April 2008 |
| Estimated Study Completion Date: | July 2009 |
| Groups/Cohorts | Assigned Interventions |
|---|---|
|
A
Antibiotic treatment
|
Drug: Antibiotic treatment
Cefuroxime 750mg X3/d, Ampicillin 2G X4/d, Flagyl 500mg X3/d, Augmentin 1G X3/d, Gentamycin 240mg X1/d, Clindamycin 600mg X3/d, Ciprofloxacin 400mg X2/d All drugs will be administered IV until clinical improvement.
|
|
B
Non antibiotic treatment
|
Drug: No antibiotics
Allowed medications for both groups will include PPI / H2 blockers, home medication, SC insulin for diabetes, and SC clexane if indicated.
|
Cholelithiasis and inflammatory biliary tract disease constitute a major health problem in western countries. Acute cholecystitis is the third major cause of emergency admission to a surgical ward and its incidence increases with increasing age. Acute cholecystitis is defined as acute inflammation of the gallbladder which is commonly caused by gallstones which are impacted in the cystic duct. The treatment of acute cholecystitis varies between different medical centers around the world. In some hospitals, mainly in the US, the most common treatment is early laparoscopic cholecystectomy within 72 hours from the onset of symptoms / admission. However, in the UK and many other centers in Europe the treatment of acute cholecystitis is conservative (NPO, IV fluids and antibiotics) and laparoscopic cholecystectomy is delayed. The reasons for delayed surgery differ between institutions and include the assumption of decreased complications, surgeon and OR availability and schedule, costs, and hospital policy.
A recent metanalysis proved similar safety and efficacy of early and delayed laparoscopic cholecystectomy. The conversion rate, length of operation and complication rate (overall complication rate, intra-abdominal collection, bile leak, and CBD injury) were also comparable.
At Hadassah-Hebrew University Medical Center, Mount Scopus patients with acute cholecystitis are treated conservatively followed by delayed laparoscopic cholecystectomy. Over the years this approach proved to carry relatively low rate of complications, mainly bile duct injuries <1%, without interruption to the busy OR schedule.
Regardless to the lack of evidence based guidelines for the treatment of acute cholecystitis the traditional triad of NPO, IV fluids and antibiotics was adopted at our institution vis-à-vis the higher complication and conversion rate for early cholecystectomy. The antibiotic treatment is associated with side effects, costs and most important unavoidable development of bacterial drug resistance. However, to date there are no randomized trials proving the superiority of either one of these methods.
Eligibility| Ages Eligible for Study: | 18 Years to 70 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
| Sampling Method: | Probability Sample |
Patients admitted through the emergency department that are diagnosed with acute cholecystits and meet the inclusion criteria will be given the opportunity to participate in the trial. Informed consent is required. Patients may withdraw from the study at any time without giving reasons and without jeopardizing further treatment.
Inclusion Criteria:
Patients with the diagnosis of mild acute cholecystitis that meet the following:
Sonographic (or CT) findings:
Additional one of the following:
Exclusion criteria:
Contacts and Locations| Contact: Haggi Mazeh, M.D. | 00 972 2 5844550 | hmazeh@hadassah.org.il |
| Israel | |
| Hadassah Medical Organization | Recruiting |
| Jerusalem, Israel, 91120 | |
| Contact: Arik Tzukert, DMD 0097226776095 arik@hadassah.org.il | |
| Contact: Hadas Lemberg, PhD 0097226777572 lhadas@hadassah.org.il | |
| Principal Investigator: | Haggi Mazeh, M.D. | Hadassah Medical Organization |
| Study Director: | Herbert R Freund, M.D. | Hadassah Medical Organization |
More Information
| Responsible Party: | Hadassah Medical Organization ( Dr. Haggi Mazeh ) |
| Study ID Numbers: | cholecystitis-HMO-CTIL |
| Study First Received: | November 11, 2007 |
| Last Updated: | February 15, 2009 |
| ClinicalTrials.gov Identifier: | NCT00557453 History of Changes |
| Health Authority: | Israel: Israeli Health Ministry Pharmaceutical Administration |
|
Gallbladder Diseases Anti-Infective Agents Anti-Bacterial Agents Digestive System Diseases Acalculous Cholecystitis |
Therapeutic Uses Biliary Tract Diseases Cholecystitis Pharmacologic Actions |