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Comparison of Subjective Experiences Between Patients Receiving Clear Aligners or Fixed Appliances

Comparison of Subjective Experiences Between Patients Receiving Clear Aligners or Fixed Appliances During the Initial Stage of Orthodontic Treatment

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03656471
Enrollment
160
Registered
2018-09-04
Start date
2013-12-03
Completion date
2016-02-01
Last updated
2018-09-04

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

Conditions

Anxiety, Pain, Quality of Life

Brief summary

This study aimed to compare experiences between adult patients receiving clear aligners and fixed appliances during the initial stage of orthodontic treatments.

Detailed description

Patients receiving either clear aligner treatments were enrolled in this study. During the same time period, patients receiving fixed orthodontic treatments well-matched with clear-aligner patients by similar ages (difference \< 3 years), same gender and similar levels of severity of malocclusion \[similar Index of Complexity Outcome and Need (ICON) level\] were enrolled.The two groups were well-matched with ages, gender and levels of malocclusion severity. Pain perception, anxiety and quality of life were assessed through visual analogue scale (VAS), state-trait anxiety inventory (STAI) and oral health impact profile-14 (OHIP-14), respectively.

Interventions

DEVICEclear aligners or fixed appliances

Patients choose clear aligners or fixed appliances to treat their malocclusions

Sponsors

West China Hospital
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Must be 18 years of age or older; * Must be in good general health; * Upper and lower arches were both involved in two groups; * The fixed appliances group must be treated with wires and brackets only with the initial arch wire of 0.012 NiTi ; * Must be willing to sign and give written informed consent in accordance with institutional and federal guidelines.

Exclusion criteria

* Once been undergoing with orthodontic treatment; * Experienced tooth ache recently; * Been diagnosed with contagious and/or systematical diseases; * Have taken any kind of painkillers three days before the initial treatment; * When Trait Anxiety Inventory (T-AI) shows a score believed to define a psychological state of over anxiety (male over 53 points and female over 55 points).

Design outcomes

Primary

MeasureTime frameDescription
The chronological changes in pain perceptionBaseline, Day 1, Day 2,Day 3,Day 4,Day 5,Day 6,Day 7,and Day 14The chronological changes in pain perception during the fortnight of orthodontic treatment were assessed through visual analogue scale (VAS). Participant is asked to place a line perpendicular to the VAS line.The score is determined by measuring the distance (mm) on the 10-cm line between the no painanchor and the patients' mask,providing a range of scores from 0-100. A higher score indicates greater pain.

Secondary

MeasureTime frameDescription
The chronological changes of anxiety levelBaseline, Day 1,Day 3,Day 5,Day 7 and Day 14Secondary outcomes concerning chronological changes of anxiety were assessed before and after orthodontic treatments through state-trait anxiety inventory (ST-AI). A higher score indicates higher anxiety level.
The chronological changes in quality of lifeBaseline,Day 1 ,Day 7 and Day 14Secondary outcomes concerning chronological changes of anxiety of life were assessed before and after orthodontic treatments through oral health impact profile-14 (OHIP-14).A higher score indicates lower quality of life.

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026