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The Clinical Evaluation of Two Different Film Thicknesses of Clear Overlay Retainer.

NCT02618330 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 80

Last updated 2015-12-03

No results posted yet for this study

Summary

The aims of this study were to compare health related quality of life, comforts degrees，retention effectiveness, and failure rates as well as survival times between two clear overlay retainers with different thicknesses, thus to provide basis information regarding appropriate selections of the thickness of clear overlay retainers.

Conditions

  • Retention

Interventions

DEVICE

retainer

24 h wearing whether 0.75-mm-thick or 1.00-mm-thick film retainer

Sponsors & Collaborators

  • Yafen Zhu

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
12 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-07-31
Primary Completion
2015-06-30

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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 NCT02618330 on ClinicalTrials.gov