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Earset Healthy Volunteer Study

NCT01611246 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 22

Last updated 2024-07-11

No results posted yet for this study

Summary

The study will recruit healthy volunteers to undergo the Iontophoresis procedure using the Acclarent Iontophoresis System with Earset (IPSES).

Conditions

  • Otitis Media

Interventions

DEVICE

Iontophoresis System With Earset

iontophoresis of lidocaine-based solution for numbing tympanic membrane

Sponsors & Collaborators

  • Acclarent

    collaborator INDUSTRY

  • Integra LifeSciences Corporation

    lead INDUSTRY

Principal Investigators

  • Joseph Roberson, M.D. · CEI Medical Group

Eligibility

Min Age
12 Months
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2012-05-01
Primary Completion
2012-08-01
Completion
2012-08-01

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01611246 on ClinicalTrials.gov