Four Arm Safety & Efficacy With Antipyrine and Benzocaine Otic Solution in Children With Acute Otitis Media
Public ClinicalTrials.gov record NCT02037893. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.
Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.
Official title
A Four-arm, Randomized, Double-blind, Active and Placebo Controlled Study to Determine the Safety and Efficacy of a Combination Antipyrine and Benzocaine Otic Solution Compared With Antipyrine Otic Solution Alone, Benzocaine Otic Solution Alone and to Placebo Otic Solution to Relieve Pain Symptoms in Children With Acute Otitis Media.
Brief summary
Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.
The primary objective is to compare the effect of treatment with a combination of ear solutions on the reduction of pain symptoms at 1 hour after dosing in children with acute otitis media.
Study identification
- NCT ID
- NCT02037893
- Recruitment status
- Completed
- Study type
- Interventional
- Phase
- Phase 2
- Enrollment
- 112 participants
Conditions and interventions
Conditions
Interventions
- Antipyrine and Benzocaine otic solution Drug
- Antipyrine Otic Solution Drug
- Benzocaine Otic Solution Drug
- Placebo Otic solution Drug
Drug
Eligibility (public fields only)
- Age range
- 2 Months to 12 Years
- Sex
- All
- Healthy volunteers
- Healthy volunteers not accepted
This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.
Study timeline
- Start date
- Nov 2013 (Type not available)
- Primary completion
- Sep 2014 (Actual)
- Completion
- Sep 2014 (Actual)
- Last update posted
- Aug 7, 2024
2013 – 2014
United States locations
- U.S. sites
- 10
- U.S. states
- 6
- U.S. cities
- 8
| Facility | City | State | ZIP | Site status |
|---|---|---|---|---|
| Desert Clinical Research | Mesa | Arizona | 85213 | — |
| Visions Clinical Research | Tucson | Arizona | 85712 | — |
| Childrens Investigational Research Program | Bentonville | Arkansas | 72712 | — |
| Visions Clinical Research | Boynton Beach | Florida | 33472 | — |
| Kentucky Pediatric and Adult Research | Bardstown | Kentucky | 40004 | — |
| Carolina Ear, Nose and Throat Clinic | Orangeburg | South Carolina | 29118 | — |
| Foothill Family Clinic | Salt Lake City | Utah | 84109 | — |
| FirstMed East | Salt Lake City | Utah | 84121 | — |
| Foothill Family Clinic South | Salt Lake City | Utah | 84121 | — |
| Jordan River Family Medicine | South Jordan | Utah | 84095 | — |
Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.
About this trial record page
- What this page shows
- Public field values for ClinicalTrials.gov record NCT02037893, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
- What this page does not do
- No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
- Where the data comes from
- Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
- Last refresh
- Last update posted Aug 7, 2024 · Synced Oct 21, 2026
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Open the official record
The complete public registry record, listed eligibility criteria, and available contact information for NCT02037893 live on ClinicalTrials.gov.