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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00147914
Other study ID # 11791A
Secondary ID
Status Completed
Phase Phase 4
First received September 2, 2005
Last updated May 1, 2017
Start date February 2005
Est. completion date February 18, 2017

Study information

Verified date May 2017
Source University of Chicago
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


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.


Recruitment information / eligibility

Status Completed
Enrollment 100
Est. completion date February 18, 2017
Est. primary completion date February 2007
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility 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.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Cefdinir (drug)
cefdinir 300mg per orally twice daily for 10 days
amoxicillin/clavulanate
1000mg /62.5mg extended release per orally twice daily for 10 days

Locations

Country Name City State
United States University of Chicago Chicago Illinois

Sponsors (1)

Lead Sponsor Collaborator
University of Chicago

Country where clinical trial is conducted

United States, 

References & Publications (2)

Tantilipikorn P, Fritz M, Tanabodee J, Lanza DC, Kennedy DW. A comparison of endoscopic culture techniques for chronic rhinosinusitis. Am J Rhinol. 2002 Sep-Oct;16(5):255-60. — View Citation

Vaidya AM, Chow JM, Stankiewicz JA, Young MR, Mathews HL. Correlation of middle meatal and maxillary sinus cultures in acute maxillary sinusitis. Am J Rhinol. 1997 Mar-Apr;11(2):139-43. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Improvement in quality of life At baseline and within 1 week of completing treatment
Primary SNOT 20 questionnaire At baseline and within 1 week of completing treatment
Secondary Clinical signs and symptoms alleviated At baseline and within 1 week of completing treatment
See also
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Completed NCT00930488 - Treatment of Patients With Acute Sinusitis N/A
Recruiting NCT03766568 - Single Use Device Endoscopy for the Diagnosis of Acute Bacterial Rhinosinusitis in Primary Care N/A
Completed NCT04588376 - Improving Antibiotic Prescribing for Pediatric Respiratory Infections by Family Physicians With Peer Comparison N/A