Phase III Study Evaluating Topical Benzocaine for Treatment of Acute Otitis Media in Children

NCT ID: NCT03116737

Last Updated: 2017-10-13

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE3
• Total Enrollment: 141 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2017-01-03
• Study Completion Date: 2017-07-21

Brief Summary

The Phase III study is designed to assess the safety, tolerability, and efficacy of Topical Benzocaine in children, ages 5 to 12 years, presenting with Acute Otitis Media-associated ear pain.

Conditions

Pain; Acute Otitis Media

Keywords

AOM

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: QUADRUPLE

Study Groups

Benzocaine Otic Solution

Group Type: EXPERIMENTAL

Benzocaine Otic Solution

Intervention Type: DRUG

Placebo

Group Type: PLACEBO_COMPARATOR

Placebo

Intervention Type: DRUG

Interventions

Benzocaine Otic Solution

Intervention Type: DRUG

Placebo

Intervention Type: DRUG

Other Intervention Names

Topical otic solution

Eligibility Criteria

Inclusion Criteria

• Male or female patients ages 5 to 12 years of age with a clinical diagnosis of unilateral AOM, and with ear pain (current episode <2 weeks duration). Baseline pain entry requires a minimum score of 4 on the FPS-R.
• Patients/guardians must provide Institutional Review Board (IRB) approved written assent, as appropriate, which must be accompanied by an IRB approved written informed consent form (ICF) from the patient's legally acceptable representative (i.e., parent or guardian), as applicable. In addition, all patients or their legally acceptable representatives (i.e., parent or guardian) must sign a Health Insurance Portability and Accountability Act (HIPAA) authorization, if applicable.
• Patients must be physically active and otherwise judged to be in good health on the basis of the medical history and a limited physical examination, as determined by the Investigator.
• Females of childbearing potential must also have a negative urine human chorionic gonadotropin (hCG) pregnancy test on the Study Day, Visit 1.

Exclusion Criteria

• Patients unable or refusing to independently and consistently complete the FPS-R pain measurements.
• Patients with bilateral AOM, perforated tympanic membrane, history of a perforated tympanic membrane in the last 6 months, or if a perforated tympanic membrane could not be ruled out by speculum examination, impedance testing tympanometry, pneumatic otoscopy, or a Valsalva maneuver.
• Patients who are subsequently diagnosed with a perforated membrane during treatment are to be discontinued immediately.
• Patients with indwelling tympanostomy tubes or draining otitis in the affected ear(s), bullous lesions, erythema of the tympanic membrane without other evidence of AOM, and patients with an anatomic defect of the ear or nasopharynx.
• Complications of treated/untreated ear disease other than qualifying AOM over the past 2 weeks.
• Patients with comorbidity requiring antibiotic therapy, allergy to study medication, immunologic deficiency, and major medical condition(s).
• Patients presenting with methemoglobinemia or a history of methemoglobinemia, vertigo, inherited enzyme deficiencies (including G6PD), impaired cardiac or respiratory functions, epilepsy, heart diseases, hypersensitivity to benzocaine or any other related drug product, inflamed or infected skin, dermatitis, previous medication related shock episode, hepatic impairment, or myasthenia gravis.
• Acute or chronic otitis externa.
• Chronic otitis media (current episode ≥ 2 weeks).
• Patients who smoke.
• Dermatitis involving the affected external ear canal or pinna.
• Any topical or systemic antibiotic received within the 14 days prior to study entry.
• Patients administered vaccinations a week prior to or on any of the Study Day Visits.
• Any ear drops, topical drying agent or over-the-counter (OTC) therapy for any ear related issue received within 36 hours prior to enrollment.
• Fever >102°F or at any elevated level considered necessary by the study investigator.
• Known hypersensitivity to the study drug or similar compounds including any of the inactive ingredients.
• Patients receiving medication on a chronic basis for pain (including steroidal or non-steroidal anti-inflammatory drugs).
• Oral analgesics such as ibuprofen/acetaminophen within 6 hours prior to study entry.
• Use of drug products with potential interactions including sulfonamides, aminosalicylates, anti-cholinesterases, suxamethonium, antiarrhythmics, monoamine oxidase inhibitors, or tricyclic antidepressants within 14 days.
• Eating, drinking, chewing of gum, or use of mints/lozenges during the first hour after initial study dose.
• Children that use pacifiers and/or are still breastfed.
• Exposure to any investigational agent within the 30 days prior to study entry.
• Previous enrollment in this study.
• Pregnant or lactating.
• Clinically significant mental or emotional illnesses (by history or as determined by the on-site investigator).
• The child has a condition or demonstrates a behavior that the Investigator or site personnel believe would interfere with the ability to provide assent (age appropriate) or comply with study instructions/tasks, or that might confound the interpretation of the study results, or put the child or others at risk.

• Minimum Eligible Age: 5 Years
• Maximum Eligible Age: 12 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Lachlan Pharma Holdings

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

Cyn3rgy Research

Gresham, Oregon, United States

Countries

United States

Other Identifiers

LP7700

Identifier Type: -

Identifier Source: org_study_id