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临床试验/NCT02554383
NCT02554383已完成3 期

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

Nader Shaikh6 个研究点 分布在 1 个国家目标入组 515 人开始时间: 2016年2月最近更新:
适应症
干预措施

试验速览

阶段
3 期
状态
已完成
发起方
入组人数
515
试验地点
6
主要终点
The Mean Pediatric Rhinosinusitis Symptom Scale (PRSS) Score Over the First 10 Days of Follow-up According to the Presence of Pathogens in the Nasopharynx at Enrollment

研究概览

简要总结

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.

详细描述

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.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
2 Years 至 11 Years(Child)
性别
All
接受健康志愿者

入选标准

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

排除标准

  • 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

研究组 & 干预措施

Treatment A

Active Comparator

Amoxicillin-clavulanate (90/6.4 mg/kg/d in 2 divided dosed for 10 days)

干预措施: Amoxicillin-clavulanate (Drug)

Treatment B

Placebo Comparator

Placebo made to match the study antibiotic will be taken bid orally for 10 days

干预措施: Placebo (Drug)

结局指标

主要结局

The Mean Pediatric Rhinosinusitis Symptom Scale (PRSS) Score Over the First 10 Days of Follow-up According to the Presence of Pathogens in the Nasopharynx at Enrollment

时间窗: Days 2 to 11

The Pediatric Rhinosinusitis Symptom Scale (PRSS) is a 8 item scale assessing symptoms of sinusitis. Parents are asked how their child has been doing over the last 24 hours by rating each of 8 symptoms - stuffy nose, runny nose, daytime cough, tiredness, irritability, trouble breathing through the nose, nighttime cough \& trouble sleeping - as none, almost none, a little, some, a lot \& an extreme amount with respective scores of 0, 1, 2, 3, 4 \& 5. The 8 ratings were summed to obtain a PRSS score. Scores ranged from 0-40. Higher scores indicate greater severity. The parent completed the scale on Day 1 (enrollment) \& electronically on diaries evenings Days 2-11. Pathogens cultured were Streptococcus pneumoniae, Haemophilus influenzae, and Moraxella catarrhalis.

The Mean Pediatric Rhinosinusitis Symptom Scale (PRSS) Score Over the First 10 Days of Follow-up According to the Presence of Colored Nasal Discharge at Enrollment

时间窗: Days 2 to 11

The Pediatric Rhinosinusitis Symptom Scale (PRSS) is a 8 item scale assessing symptoms of sinusitis. Parents are asked how their child has been doing over the last 24 hours by rating each of 8 symptoms - stuffy nose, runny nose, daytime cough, tiredness, irritability, trouble breathing through the nose, nighttime cough \& trouble sleeping - as none, almost none, a little, some, a lot \& an extreme amount with respective scores of 0, 1, 2, 3, 4 \& 5. The 8 ratings were summed to obtain a PRSS score. Scores ranged from 0-40. Higher scores indicate greater severity. The parent completed the scale on Day 1 (enrollment) \& electronically on diaries evenings Days 2-11. Nasal discharge, either yellow or green, was considered colored.

次要结局

  • The Distribution of Children Receiving a Systemic Antibiotic Over the First 10 Days of Follow-up(Days 2 to 11, where Day 1 is day of enrollment. The mean number of days of follow-up in this interval was 9.8.)
  • The Distribution of Children for Whom Diarrhea or Generalized Rash Was Reported(Day 1 through Day 23.)
  • The Distribution of Children Compliant With Study Medication(Days 1 to 11, where Day 1 is day of enrollment)
  • The Distribution of Children Experiencing Treatment Failure (TF)(Day of enrollment to the day of the follow-up visit. The mean length of actual follow-up was 13.4 days. For each child with incomplete follow-up, multiple imputation was used and PRSS scores for the remaining days were imputed.)
  • The Distribution of Children Developing Acute Otitis Media (AOM) Over the First 10 Days of Follow-up(Days 2 to 11, where Day 1 is day of enrollment. The mean number of days of follow-up in this interval was 9.8.)

研究者

发起方
Nader Shaikh
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Nader Shaikh

Associate Professor of Pediatrics, University of Pittsburgh School of Medicine

University of Pittsburgh

研究点 (6)

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