Clinical Trials Logo

Clinical Trial Summary

The aim of the study is to investigate the possible influence of different durations of use of postoperative elastic bandaging (seven days vs. thirty days) in the results of otoplasty. We hypothesize that the duration of elastic bandage use has no significant influence on the incidence of relapse of prominence of the ears and need for reoperation.


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Caregiver, Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT01810497
Study type Interventional
Source University of Campinas, Brazil
Contact
Status Completed
Phase N/A
Start date May 2012
Completion date March 2015

See also
  Status Clinical Trial Phase
Completed NCT03194269 - Long Term Prospective Uncontrolled Study Of Earfold™ For The Treatment Of Prominent Ears Phase 4