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Efficacy of Antibiotics in Children With Acute Sinusitis: Which Subgroups Benefit?

N

Nader Shaikh

Status and phase

Completed
Phase 3

Conditions

Respiratory Tract Infections
Sinusitis

Treatments

Drug: Amoxicillin-clavulanate
Drug: Placebo

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT02554383
STUDY20110386
U01AI118506 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

The objective of this trial is to determine whether certain subgroups of children with acute sinusitis exist in whom antibiotic therapy can be appropriately withheld.

Full description

The current clinical practice guideline from the American Academy of Pediatrics for the Diagnosis and Management of Acute Bacterial Sinusitis recommends that the diagnosis of acute sinusitis is made when symptoms of an upper respiratory infection (URI) persist beyond 10 days without showing signs of improvement (persistent presentation), when symptoms appear to worsen (on the 6th to 10th day) after a period of improvement (worsening presentation), or when both high fever and purulent nasal discharge are present concurrently for at least 3 consecutive days (severe presentation). In studies to date, children with persistent and worsening presentations comprise >95% of cases. The investigators preliminary data and the available literature suggest that only a subset of children being diagnosed with acute sinusitis on the basis of current criteria are likely to have bacterial disease. This is not entirely surprising because current criteria rely solely on the duration and the quality of respiratory tract symptoms (which are both common and non-specific). Accordingly, it seems likely that many children currently being diagnosed as having acute sinusitis actually have an uncomplicated upper respiratory infection. This is important because acute sinusitis is one of the most common diagnoses for which antimicrobials are prescribed for children in the United States, accounting for 7.9 million prescriptions annually. A critical need thus exists to establish which subgroups of children currently being diagnosed with acute sinusitis actually benefit from antimicrobial therapy.

The objective of this trial is to determine whether certain subgroups of children with acute sinusitis exist in whom antibiotic therapy can be appropriately withheld. This objective will be achieved by conducting a large, randomized, double-blind, placebo-controlled clinical trial in children 2 to 12 years of age with persistent or worsening presentations of acute sinusitis. Based on the investigators preliminary data, the investigators hypothesize that only certain subgroups of children currently being treated for acute sinusitis actually benefit from antimicrobial therapy. By identifying, in a large placebo-controlled trial, subgroups of children who respectively do and do not benefit from antimicrobial therapy, the investigators will be better able to determine which children should be classified as having acute bacterial sinusitis. Accordingly, the results of this trial may impact not only the treatment guidelines for acute sinusitis but also the diagnostic criteria, and will help ensure that, to the extent possible, antibiotic use is limited to appropriate patients. This, in turn, will maximize the likelihood of achieving optimal outcomes and minimize the risk of promoting antibiotic resistance.

Enrollment

515 patients

Sex

All

Ages

2 to 11 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Meets criteria for "persistent" or "worsening" presentations of sinusitis
  • Baseline score ≥9 on the Pediatric Rhinosinusitis Symptom Scale

Exclusion criteria

  • Severe presentation (≥3 days of colored nasal discharge and fever ≥39°C
  • Asthma/allergic rhinitis explains symptoms
  • Allergy to amoxicillin-clavulanate
  • Immotile cilia syndrome
  • Cystic fibrosis
  • Immunodeficiency
  • Parental inability to read/write English or Spanish
  • Other concurrent infection (e.g., pneumonia, acute otitis media, streptococcal pharyngitis)
  • Systemic toxicity
  • Wheezing on exam
  • Antibiotic use within 15 days

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

515 participants in 2 patient groups, including a placebo group

Treatment A
Active Comparator group
Description:
Amoxicillin-clavulanate (90/6.4 mg/kg/d in 2 divided dosed for 10 days)
Treatment:
Drug: Amoxicillin-clavulanate
Treatment B
Placebo Comparator group
Description:
Placebo made to match the study antibiotic will be taken bid orally for 10 days
Treatment:
Drug: Placebo

Trial documents
1

Trial contacts and locations

6

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Data sourced from clinicaltrials.gov

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