跳至主要内容
临床试验/NCT00419380
NCT00419380已完成4 期

Treatment of Clogged Tympanostomy Tubes: An Off-Label Use of Dornase Alfa (Pulmozyme®)

University of Colorado, Denver1 个研究点 分布在 1 个国家目标入组 41 人开始时间: 2007年1月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
已完成
入组人数
41
试验地点
1
主要终点
Patency of the Tympanostomy Tube at the Day-14 Visit.

研究概览

简要总结

The purpose of this study is to evaluate Pulmozyme® (dornase) as compared to a standard ear drop Floxin® (ofloxicin) to dissolve clogged tubes. This study will monitor the use of the new drug for any problems related to the medication. Patients are being asked to be in this study because they had tubes placed for the treatment of chronic ear infection and the tube(s) are now clogged. Clogged tubes are a common problem found in children with tubes. This problem occasionally is improved with ear drops like Floxin®. However, it is frequently not improved even after this standard ear drop treatment.

详细描述

The success in treating blocked tubes may relate to the ability to dissolve the material clogging the tube as well as dealing with the thick fluid in the middle-ear. The reasoning behind this study is that the use of Pulmozyme® may be able to treat both of these problems. Pulmozyme® was approved by the FDA in 1994 for the treatment of cystic fibrosis patients. Infections present in airway (lung) secretions of cystic fibrosis patients and the material that plugs ear tubes are in some ways the same. "Off-label" use of a drug is the practice by physicians to use a FDA-approved drug in treating conditions other than what the original approval was intended for. Pulmozyme® has been used to treat other lung diseases not related to cystic fibrosis. There has been no published report on the use of Pulmozyme® to treat ear infections. This study is a clinical trial that compares two treatments and will last for 3 months.

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
Single (Investigator)

入排标准

年龄范围
1 Year 至 18 Years(Child, Adult)
性别
All
接受健康志愿者
是

入选标准

  • •subjects from age 1 to 18 years who have undergone tube placement in the previous 9 months.
  • •subjects with middle-ear fluid on entry into the study will be required to have had a prior normal hearing test.

排除标准

  • •subjects with symptoms of an acute otitis media (otalgia or otorrhea), sensorineural hearing loss,cranio-facial syndromes, cystic fibrosis, prior ear surgery except tube placement, sensitivity to fluoroquinolones and presence of granulation tissue in the lumen of the tympanostomy tubes will be excluded.

研究组 & 干预措施

dornase alfa (Pulmozyme®)

Active Comparator

dornase alfa - Pulmozyme®: 5 drops twice daily for 7 days to the affected ear.

干预措施: dornase alfa (Pulmozyme®) (Drug)

Ofloxin

Active Comparator

Ofloxin : 5 drops twice daily for 7 days to the affected ear.

干预措施: dornase alfa (Pulmozyme®) (Drug)

结局指标

主要结局

Patency of the Tympanostomy Tube at the Day-14 Visit.

时间窗: 14 days

次要结局

  • Presence or Absence of Drainage in the Ear Canal and Fluid in the Middle Ear at the the Day-14 Visit.(14 days)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

Loading locations...

相似试验