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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00622518
Other study ID # 33097-B
Secondary ID 07-9092-B 01
Status Completed
Phase N/A
First received February 13, 2008
Last updated November 4, 2010
Start date February 2008
Est. completion date April 2009

Study information

Verified date November 2010
Source University of Washington
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

The purpose of this study is to determine if a commercially available homeopathic ear drop preparation is effective in reducing symptoms in children 6 months - 11 years old with acute otitis media. A total of 120 study patients with otitis media will be randomized to receive homeopathic ear drops, or no ear drops, in addition to receiving standard care. It is postulated that children using the ear drops will have more rapid resolution of symptoms and need fewer antibiotics than those randomized to not receive the ear drops.


Recruitment information / eligibility

Status Completed
Enrollment 119
Est. completion date April 2009
Est. primary completion date February 2009
Accepts healthy volunteers No
Gender Both
Age group 6 Months to 11 Years
Eligibility Inclusion Criteria:

- Presenting to participating clinic with otitis media

- Diagnosed with acute otitis media

- Parents rate symptoms as a "moderate problem" or more

Exclusion Criteria:

- Diagnosis of otitis media within preceding 30 days

- Receipt of antibiotics within 2 days

- Perforated ear drum or bullous lesion

- Receipt of homeopathic treatment within 30 days

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Supportive Care


Related Conditions & MeSH terms


Intervention

Drug:
Hyland's earache drops
3-4 drops in affected ear 3 times a day as needed for up to 5 days

Locations

Country Name City State
United States University of Washington Medical Center-Roosevelt Pediatric Care Center Seattle Washington

Sponsors (2)

Lead Sponsor Collaborator
University of Washington Standard Homeopathic Company

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Resolution of Otitis Media Symptoms Mean scores as measured on the Ear Treatment Group-5 scale. This scale quantifies severity of symptoms in children with otitis media. There are 5 components to the scale: fever, earache or tugging, feeding, irritability and sleep. For each component symptoms are rated as 0, 4 or 7 based on severity, with higher scores indicating more sever symptoms. For the primary outcome, the scores for each component were summed to determine an overall Ear Treatment Group -5 Scale score. Total scores range from 0-35. Two assessessments were conducted each day. 5 days No
Secondary Side Effects of Therapy 5 days Yes
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