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Comparison Study Between Cefdinir & Amoxicilline/Clavulanate in Acute Sinusitis and Assessment of Quality of Life
This study is ongoing, but not recruiting participants.
Sponsored by: University of Chicago
Information provided by: University of Chicago
ClinicalTrials.gov Identifier: NCT00147914
  Purpose

This study is a comparison between two commonly used antibiotics (Cefdinir vs. Amoxicillin/Clavulanate) in patients with acute sinus infection, surveying quality of life. The hypothesis is that the two treatments would be at the least equivalent based on clinical outcome measures of improvement in quality of life.


Condition Intervention Phase
Acute Bacterial Sinusitis
Drug: Amoxicillin/Clavulanate (drug), Cefdinir (drug)
Phase IV

MedlinePlus related topics: Sinusitis
Drug Information available for: Amoxicillin Amoxicillin sodium Amoxicillin trihydrate Clavulanic acid Cefdinir
U.S. FDA Resources
Study Type: Interventional
Study Design: Treatment, Randomized, Double-Blind, Dose Comparison, Parallel Assignment, Efficacy Study
Official Title: A Comparison Study Between Cefdinir and Amoxicilline/Clavulanate in Patients With Acute Sinusitis and Assessment of Quality of Life (QOL)

Further study details as provided by University of Chicago:

Primary Outcome Measures:
  • Improvement in quality of life
  • SNOT 20 questionnaire

Secondary Outcome Measures:
  • Clinical signs and symptoms alleviated

Estimated Enrollment: 100
Study Start Date: February 2005
Estimated Study Completion Date: May 2006
Detailed Description:

The purpose if this investigation is to evaluate the rate of improvement ub Quality of LIfe (QOL) in two different medications, a 10-day course of Cefdinir 300 mg PO BID versus a 10-day course of Amoxicillin/Clavulanate 1000 mg/62.5 mg XR BID, in the treatment of acute bacterial sinusitis.

  Eligibility

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

Inclusion Criteria:

  • Male and female outpatient adults greater than 18 years old fulfilling the case definition for acute bacterial sinusitis
  • Case definition includes clinical signs and symptoms, radiographic findings and collection of purulent material from the sinus

Exclusion Criteria:

  • Symptoms less than 7 days and more than 3 weeks
  • History of sinus surgery within 3 months
  • History of frequent sinus infections (more than 2 episodes within the last 6 months)
  • History of kidney and liver disease
  • Pregnant and nursing women
  • Pre-existing disease that could predispose to sinus infections (cystic fibrosis or nasal polyps
  • Immunosuppressed patients
  • History of allergy to either drug. Patients with a documented history of allergies to either penicillin or cephalosporins will be excluded.
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00147914

Locations
United States, Illinois
University of Chicago
Chicago, Illinois, United States, 60637
Sponsors and Collaborators
University of Chicago
Investigators
Principal Investigator: Jacquelynne Corey, M.D. University of Chicago
  More Information

Publications:
Study ID Numbers: 11791A
Study First Received: September 2, 2005
Last Updated: March 12, 2007
ClinicalTrials.gov Identifier: NCT00147914  
Health Authority: United States: Institutional Review Board

Keywords provided by University of Chicago:
Acute bacterial sinusitis

Study placed in the following topic categories:
Amoxicillin
Otorhinolaryngologic Diseases
Respiratory Tract Infections
Respiratory Tract Diseases
Cefdinir
Clavulanic Acid
Clavulanic Acids
Quality of Life
Sinusitis
Amoxicillin-Potassium Clavulanate Combination

Additional relevant MeSH terms:
Anti-Infective Agents
Anti-Bacterial Agents
Molecular Mechanisms of Pharmacological Action
Paranasal Sinus Diseases
Therapeutic Uses
Enzyme Inhibitors
Pharmacologic Actions
Nose Diseases

ClinicalTrials.gov processed this record on January 16, 2009