Safety and Efficacy of Sinuclean Nebules 45 (Class 1 Medical Device) in the Treatment of Pediatric Exudative Otitis Media, Randomized, Double Blind, Comparative, Parallel Study
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 发起方
- 入组人数
- 70
- 试验地点
- 2
- 主要终点
- Resolution of tympanic effusion
研究概览
简要总结
The goal of the study is to investigate if the active agent of Sinuclean Nebules is efficacious in the treatment of pediatric exudative otitis media, comparing with saline.
Sinuclean Nebules is a solution of cucurbitacins B,D,I,E (glycosylated triterpenes) 45 mcg, extracted from Ecballium Elaterium.
详细描述
Eligible pediatric subjects with diagnosis of mono or bi-lateral exudative otitis media (obtained with otorhinolaryngologic endoscopic examination, tympanogram and tonal audiometry), are randomized to treatment with Sinuclean Nebules 45 or saline.
Treatment is administered by trained caregiver with nebulizer (Rinowash Nasal Shower): one nebulization/nostril/day for two cycles of 10 consecutive days. Cycles are interrupted by a period of 7 days.
Visits 1 Baseline T0: confirmation of eligibility, randomization, training of caregiver, dispensation of blinded therapy for two cycles, delivery of the clinical diary.
Visit 2 after 10 days of therapy + 7 days of interval: phone call to check for adverse events, therapy adherence, concomitant diseases and treatments, and to prescribe second cycle of therapy.
Visit 3 End of Study: assessment of the exudative otitis media with otorhinolaryngologic endoscopic examination, tympanogram tonal audiometry, verification of the subject's clinical diary.
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
- 3 Years 至 10 Years（Child）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Documented diagnosis of mono or bi-lateral exudative otitis media, performed the day of recruitment or in the week before, with endotympanic effusion present for at least 3 months, and hearing loss.
- •The diagnostic criteria is type B tympanogram for at least one of the two ears.
- •The criteria is integrated by a) tonal audiometry to demonstrate bilateral or monolateral deficit (loss of more than 20dB averaged to 0.5-1.2 and 4Khz in the best ear with pure tone audiometry); for 1-3 yo subjects the audiometry is behavioural b) otorhinolaryngologic examination in endoscopy for the otologic, rhino-sinusal and pharyngeal districts.
排除标准
- •Outcomes of adenotonsillectomy
- •Velo-palatal insufficiencies, cleft lip and cleft palate.
- •Hearing loss of perceptual, and mixed type.
- •Clinical conditions (systemic diseases or other) that may interfere with the evaluation of safety and clinical effectiveness of the product under investigation, for example: diabetes mellitus, heart disease, chronic renal failure, active systemic infections)
- •Assumption, during the study of drugs that may interfere with the assessment of the product object of clinical investigation.
- •Possibility of needing treatment during the study with drugs that are not allowed, for example: antibiotics in long-term prophylaxis, immunosuppressants, corticosteroids.
- •Regular intake of steroids in the four weeks preceding the date of the admission visit.
- •Viral or allergic rhinitis, with active effusion.
- •Down Syndrome
- •Diagnosis of immotile cilia syndrome
- •Condition of immune deficiency disease or otherwise.
- •Cystic Fibrosis.
- •Dental malocclusion
- •Other diseases of other organ systems, which, in the opinion of the investigator, may interfere with the purpose or the study procedures.
- •Not vaccinated subjects, with no clinical history of varicella who have been in contact, in the 4 weeks before the admission visit, with people who may be suffering from chicken pox or Zoster.
- •Psychic condition incompatible with participation in the research.
- •History of intolerance or allergy to the components of Sinuclean Nebules.
- •Medical and surgical intervention that may prejudice the complete execution of the trial, in the 4 weeks preceding the signing of informed consent.
- •Imminence of a medical-surgical procedure that can jeopardize the completion of the trial.
- •Participation in the course to other clinical investigations, or terminated within 30 days of the start of this trial.
- •Previous randomization in the study
- •Be first- or second-grade relative of a member of the Site study staff.
结局指标
主要结局
Resolution of tympanic effusion
时间窗: At Day 28 after start of treatment
The resolution of the tympanic effusion will be assessed with tympanogram (% of subjects with type A tympanogram).
次要结局
- Complete auditory recovery(At Day 28 after start of treatment)