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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02618330
Enrollment
80
Registered
2015-12-01
Start date
2013-07-31
Completion date
Unknown
Last updated
2015-12-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Retention

Brief 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.

Interventions

DEVICEretainer

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

Sponsors

Yafen Zhu
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
12 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients after active orthodontic treatment; * Must be healthy without systemic and oral diseases; * The central incisors, canines and first molars of both upper and lower arches must be existed; * Agreed to the trial and signed informed consent forms, either by themselves, or their parents.

Exclusion criteria

* Oral habits such as bruxism and clenching, * Do not accept this type of retainers

Design outcomes

Primary

MeasureTime frame
Survival times via recording to the patients' re-visitone year

Secondary

MeasureTime frame
SF-36 scale for Quality of lifeone month
Comfort degrees assessed through Visual Analog Scoreone month
Retention effectiveness assessed according to 3D modelsone year

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 10, 2026