Full Text View  
  Tabular View  
  Contacts and Locations  
  No Study Results Posted  
  Related Studies  
A Study Comparing Safety and Efficacy of Levofloxacin and Metronidazole Versus Piperacillin/Tazobactam in Treating Complicated Appendicitis
This study has been terminated.
Sponsors and Collaborators: Johnson & Johnson Pharmaceutical Research & Development, L.L.C.
PriCara, Unit of Ortho-McNeil, Inc.
Information provided by: Johnson & Johnson Pharmaceutical Research & Development, L.L.C.
ClinicalTrials.gov Identifier: NCT00236912
  Purpose

The purpose of this study is to compare the efficacy and safety of two treatment regimens in treating patients with complicated appendicitis. Appendicitis requires antibiotic treatment when the appendix ruptures (complicated appendicitis). This is a study comparing intravenous (IV) antibiotic therapy of levofloxacin/metronidazole versus piperacillin/tazobactam for 4 to 14 days. Patients may be switched to oral therapy after 48 hours, at the doctor's discretion.


Condition Intervention Phase
Appendicitis
Drug: levofloxacin; metronidazole
Phase IV

MedlinePlus related topics: Antibiotics Appendicitis
Drug Information available for: Metronidazole Metronidazole hydrochloride Metronidazole phosphate Levofloxacin Ofloxacin Ofloxacin hydrochloride Piperacillin Piperacillin sodium Tazobactam
U.S. FDA Resources
Study Type: Interventional
Study Design: Treatment, Randomized, Open Label, Parallel Assignment, Safety/Efficacy Study
Official Title: A Multi-Center, Open-Label, Randomized Study to Compare the Safety and Efficacy of Once Daily Levofloxacin Along With Once Daily Metronidazole Versus Piperacillin/Tazobactam in the Treatment of Complicated Appendicitis

Further study details as provided by Johnson & Johnson Pharmaceutical Research & Development, L.L.C.:

Primary Outcome Measures:
  • Clinical success at the post-therapy visit; safety by adverse events.

Secondary Outcome Measures:
  • Clinical and microbiologic response at post-therapy and post-study; costs associated with care.

Estimated Enrollment: 420
Study Start Date: July 2003
Study Completion Date: September 2004
Detailed Description:

Appendicitis may be classified as uncomplicated (the appendix has not ruptured) or complicated (the appendix has ruptured or gangrene has begun). Typically all patients with complicated appendicitis are treated with intravenous (IV, through a vein) antibiotic therapy. This is a multicenter, open-label, randomized study of patients who have complicated appendicitis. Prior to surgery, patients will be randomized to either the levofloxacin/metronidazole IV group (given once daily) or the piperacillin/tazobactam IV group (given 4 times daily) and will be started on study drug. Patients who are confirmed during surgery to have complicated appendicitis, will continue to receive study drug to complete a total of 4-14 days of therapy. Those found to have uncomplicated appendicitis will stop taking study drug and be discontinued from the study. Patients may be switched after 48 hours to oral therapy, at the doctor's discretion. Patients randomized to levofloxacin/metronidazole will be switched to oral levofloxacin/metronidazole given once daily. Patients randomized to piperacillin/tazobactam will be switched to oral amoxicillin/clavulanate acid given twice daily. While in the hospital, daily assessments will be made of the patient for clinical signs and symptoms of post-operative wound infection. In addition, temperature, vital signs, pertinent physical findings, white blood count (until normal), and tests for infection will be assessed daily while in the hospital. Wound assessments and laboratory tests will be performed on the last visit as an outpatient. The main objective of this study is to determine the safety and effectiveness of the regimen containing levofloxacin and metronidazole compared with the regimen of piperacillin/tazobactam in the treatment of complicated appendicitis.

Levofloxacin 750 mg IV (through a vein) or orally then metronidazole 1500 milligrams IV (or tablet form by mouth) once daily for 4 to 14 days; or piperacillin/tazobactam 3.375 grams IV every 6 hours (or amoxicillin/clavulanate acid 875/125 milligram tablets by mouth every 12 hours) for 4 to 14 days

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Two or more symptoms of acute appendicitis for at least 24 hours or radiologic evidence of complicated appendicitis
  • Able to take medicine orally after recovering from surgery
  • If female, using birth control

Exclusion Criteria:

  • History of allergy to any study medication
  • Life expectancy < 72 hours
  • APACHE II (health) score > 25
  • Neutropenic (low white blood cell count)
  • HIV positive with current or past CD4 count < 200/mm^3
  • Low platelet count (bleeds easily)
  • Malnourished with low albumin
  • Condition requiring use of major tranquilizers
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00236912

Sponsors and Collaborators
Johnson & Johnson Pharmaceutical Research & Development, L.L.C.
PriCara, Unit of Ortho-McNeil, Inc.
Investigators
Study Director: Johnson & Johnson Pharmaceutical Research and Development, L.L.C. Clinical Trial Johnson & Johnson Pharmaceutical Research & Development, L.L.C.
  More Information

A Multicenter, Open-Label, Randomized Study to Compare the Safety and Efficacy of Once Daily Levofloxacin Along With Once Daily Metronidazole Versus Piperacillin/Tazobactam in the Treatment of Complicated Appendicitis  This link exits the ClinicalTrials.gov site

Study ID Numbers: CR002656
Study First Received: October 7, 2005
Last Updated: April 24, 2008
ClinicalTrials.gov Identifier: NCT00236912  
Health Authority: United States: Food and Drug Administration

Keywords provided by Johnson & Johnson Pharmaceutical Research & Development, L.L.C.:
complicated appendicitis
appendicitis
infection
antibiotics

Study placed in the following topic categories:
Metronidazole
Digestive System Diseases
Gastrointestinal Diseases
Appendicitis
Ofloxacin
Tazobactam
Piperacillin
Piperacillin-tazobactam combination product
Intestinal Diseases
Gastroenteritis

Additional relevant MeSH terms:
Anti-Infective Agents
Antiprotozoal Agents
Molecular Mechanisms of Pharmacological Action
Physiological Effects of Drugs
Enzyme Inhibitors
Anti-Infective Agents, Urinary
Renal Agents
Pharmacologic Actions
Cecal Diseases
Anti-Bacterial Agents
Antiparasitic Agents
Radiation-Sensitizing Agents
Therapeutic Uses
Nucleic Acid Synthesis Inhibitors

ClinicalTrials.gov processed this record on January 16, 2009