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临床试验/NCT02567825
NCT02567825已完成不适用

Efficacy of Tympanostomy Tubes for Children With Recurrent Acute Otitis Media

Alejandro Hoberman2 个研究点 分布在 1 个国家目标入组 250 人开始时间: 2015年11月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
250
试验地点
2
主要终点
The Rate of Occurrence of Acute Otitis Media (AOM) Episodes Per Child-Year

研究概览

简要总结

To determine whether tympanostomy tube placement (TTP) compared with nonsurgical management will meaningfully improve children's acute otitis media (AOM) experience over the succeeding 2 years.

详细描述

Tympanostomy tube placement (TTP) for recurrent acute otitis media (rAOM) is frequently performed in children under 3 years of age; however, a critical need exists to establish its risk/benefit ratio. Seventy percent of children experience at least one episode of AOM during the first year of life; 20% of children have rAOM. The efficacy of TTP for preventing rAOM, assumedly by maintaining middle-ear ventilation, remains unclear. Benefits of TTP must be balanced against risks of anesthesia, complications and sequelae of surgery, and cost. Accordingly, the objective of this proposal is to determine the efficacy of TTP in children aged 6-35 months, the group in which rAOM is most troublesome. The central hypothesis is that in children with rAOM, the operation will prove effective over the ensuing 2 years overall, but the benefit in a more severely affected, and therefore higher-risk subgroup may be substantially greater than in a less severely affected subgroup, in whom benefits may not outweigh risks. The rationale for this research is based on a belief that the limited nature of the benefit of TTP found in earlier clinical trials may have been the result of enrolling children whose illnesses had not been diagnosed using stringent criteria and/or whose ascertainment of episodes had relied on undocumented histories. The primary objective is to determine the extent to which TTP reduces the overall rate of recurrences in children with rAOM over a 2-year period. In a randomized, clinical trial, children aged 6-35 months who are at risk for rAOM will be followed prospectively and examined promptly with new respiratory illnesses to accurately document episodes of AOM. A total of 240 children who meet stringent inclusion criteria for rAOM will be eligible to undergo randomization within strata (age and exposure to other children) to receive TTP or nonsurgical management. Children will be followed for 2 years; the average number of episodes of AOM will be documented and compared between groups. The secondary objective is to determine changes following TTP in nasopharyngeal (NP) colonization with resistant bacteria. At the time of randomization and 3 times a year for 2 years, NP specimens will be obtained and cultured. Susceptibility testing and serotyping will be performed, and the proportions of children colonized with resistant bacteria compared between treatment groups. The tertiary objective is to determine cost-effectiveness of TTP. The investigators will calculate both direct medical and nonmedical costs and correlate this with the number of days that each child has AOM symptoms, otorrhea, and any adverse events or complications. The proposed research is innovative, as the investigators will document AOM episodes prospectively using stringent diagnostic criteria and obtain digital tympanic membrane images otoendoscopically to enhance accuracy of observations. Findings of the proposed study will provide clinicians and parents with dependable evidence concerning the overall effects of TTP compared with nonsurgical management in children with rAOM of varying degrees of severity, enabling evidence-based decisions regarding an important component of the children's healthcare.

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
None

盲法说明

Subjects in the randomization phase of the study will be randomized to either medical management or tube surgery. No masking will occur.

入排标准

年龄范围
6 Months 至 35 Months(Child)
性别
All
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

研究组 & 干预措施

Surgical Management

Active Comparator

Tympanostomy Tube Placement Topical antimicrobial treatment of acute otitis media episodes with ofloxacin drops

干预措施: Tympanostomy tube placement (Device)

Surgical Management

Active Comparator

Tympanostomy Tube Placement Topical antimicrobial treatment of acute otitis media episodes with ofloxacin drops

干预措施: Ofloxacin Otic (Drug)

Non-Surgical Management

Other

Antimicrobial treatment of acute otitis media episodes with amoxicillin-clavulanate and/or ceftriaxone

干预措施: Amoxicillin-Clavulanate and/or Ceftriaxone (Drug)

结局指标

主要结局

The Rate of Occurrence of Acute Otitis Media (AOM) Episodes Per Child-Year

时间窗: Day 1 until Day 786. The mean length of actual follow-up was 662 days / 1.8 years. For each child with incomplete 2-year follow-up, multiple imputation was used and values for the remaining days/years were imputed.

An episode of AOM is considered a discrete occurrence if symptoms and signs persisted for, or recurred, 17 or more days after the start of antimicrobial treatment. The rate is calculated by dividing the total number of occurrences by the total number of years of follow-up. Multiple imputation was used when follow-up was incomplete.

次要结局

  • The Distribution of Nonsusceptible Nasopharyngeal or Throat Pathogens Recovered at Episodes of AOM(Day 1 until Day 786.)
  • The Distribution of Nonsusceptible Nasopharyngeal or Throat Pathogens Recovered at Routine Non-Illness Visits(Day 1 until Day 786.)
  • The Distribution of Parent Reports Indicating At Least One Health Care Encounter Since the Previous Study Visit as an Indicator of Medical Resource Use(Day 1 until Day 786.)
  • The Distribution of Reported Occurrences of a Parent Missing Work Due to Child's Illness, as an Indicator of Non-Medical Resource Use(Day 1 until Day 786.)
  • The Distribution of Reported Occurrences of the Need for Special Childcare Arrangements Due to Child's Illness, as an Indicator of Non-Medical Resource Use(Day 1 until Day 786.)
  • The Mean Scores on the 6 Item Quality of Life Survey Questionnaire (OM-6)(Day 1 until Day 786.)
  • The Mean Scores on the 6 Item Caregiver Impact Questionnaire (CIQ)(Day 1 until Day 786.)
  • The Total Cost of Management of Recurrent Acute Otitis Media Per Quality Adjusted Life Days (QALDs) as a Measure of Cost-Effectiveness(Day 1 until Day 786. The mean length of actual follow-up was 662 days / 1.8 years.)
  • The Total Cost of Management of Recurrent Acute Otitis Media Per Quality Adjusted Life Days (QALDs) as a Measure of Cost-Effectiveness According to the Estimated Risk of Acute Otitis Media Recurrences at Enrollment(Day 1 until Day 786. The mean length of actual follow-up was 662 days / 1.8 years.)
  • The Rate of Occurrence of Acute Otitis Media (AOM) Episodes Per Child-Year According to the Estimated Risk of Acute Otitis Media (AOM) Recurrences at Enrollment(Day 1 until Day 786. The mean length of actual follow-up was 662 days / 1.8 years. For each child with incomplete 2-year follow-up, multiple imputation was used and values for the remaining days/years were imputed.)
  • The Frequency Distribution of AOM Episodes Among Children Completing the Study(Day 1 until Day 786. For children completing the study, the mean length of follow-up was 726 days.)
  • The Distribution of Children Experiencing Treatment Failure (TF)(Day 1 until Day 786.)
  • The Time to the First Episode of AOM(Day 1 until Day 786. The mean length of follow-up was 662 days / 21.8 months.)
  • The Mean Days Per Year Children Experience Tube Otorrhea(Day 1 until Day 786. The mean length of follow-up was 662 days / 1.8 years.)
  • The Mean Days Per Year Children Experience AOM Symptoms With an Intact Tympanic Membrane (TM)(Day 1 until Day 786. The mean length of follow-up was 662 days / 1.8 years.)
  • The Distribution of AOM Episodes Categorized as Probably Severe or Probably Nonsevere(Day 1 until Day 786.)
  • The Distribution of AOM Episodes Presenting With Tympanic Membrane Bulging or Otorrhea(Day 1 until Day 786.)
  • The Distribution of Children for Whom Protocol-Defined Diarrhea (PDD) Was Reported(Day 1 until Day 786.)
  • The Distribution of Children With a Penicillin-Nonsusceptible Nasopharyngeal or Throat Isolate At Any Follow-up Visit According to the Colonization Status at Enrollment(Day 1 until Day 786.)
  • The Mean Days Per Year Children Receive Systemic Antimicrobials for AOM(Day 1 until Day 786. The mean length of follow-up was 662 days / 1.8 years.)
  • The Distribution of Children for Whom Diaper Dermatitis Was Reported(Day 1 until Day 786.)
  • The Distribution of Children for Whom Tube Otorrhea Was Reported(Day 1 until Day 786.)
  • The Distribution of Nonsusceptible Nasopharyngeal or Throat Pathogens Recovered at AOM Episodes Late During the Respiratory Season (April-May)(April 1 to May 31, each of the 2 years of follow-up. The mean length of follow-up was 111 days / 3.7 months.)
  • The Mean Score Representing Parental Satisfaction With Clinical Management(The end-of-study visit. The mean day for this visit was 726.)

研究者

发起方
Alejandro Hoberman
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Alejandro Hoberman

Professor of Pediatrics

University of Pittsburgh

研究点 (2)

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