Effect of Clear Aligner Wear Protocol on External Root Resorption
1 other identifier
interventional
52
1 country
1
Brief Summary
The aim of this two-arm randomized clinical trial was to compare the effect of 7-day and 14-day orthodontic clear aligner wear protocols on external apical root resorption (EARR) and pain perception
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Feb 2025
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
February 2, 2025
CompletedFirst Submitted
Initial submission to the registry
January 15, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 1, 2026
CompletedFirst Posted
Study publicly available on registry
April 13, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
May 15, 2026
CompletedApril 13, 2026
April 1, 2026
1.2 years
January 15, 2026
April 3, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Root resorption
Peri-apical radiographs will be taken before and after the treatment, tooth root length will be measured before and after treatment from the radiographs
6 months
Secondary Outcomes (1)
Pain perception
After 24 hours, 1 week, 2 weeks, 1 month, 3 months and 6 months
Study Arms (2)
7-day aligner wearing protocol
ACTIVE COMPARATOR14-day aligner wearing protocol
ACTIVE COMPARATORInterventions
One group should change the orthodontic clear aligner every week (7 days) and the second group every two weeks (14 days)
Eligibility Criteria
You may qualify if:
- Participants with complete permanent dentition except wisdom teeth
- Participants presented with mild to moderate malocclusion (Average degree of crowding).
- Participants with good oral hygiene and absence of periodontal disease.
- No history of trauma or prior orthodontic treatment.
You may not qualify if:
- Participants with thin or petite roots.
- Participants with pre-existing root resorption
- Participants with endodontically treated incisors or canines.
- Participants with history of trauma to incisors teeth
- Participants with previous orthodontic treatment.
- Participants with periapical pathology, ankylosisor cystic lesions.
- Participants with medical conditions that may affecting pain or inflammatory responses.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
postgraduate orthodontic clinics at JUST
Irbid, 22110, Jordan
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Purpose
- DIAGNOSTIC
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
January 15, 2026
First Posted
April 13, 2026
Study Start
February 2, 2025
Primary Completion
April 1, 2026
Study Completion
May 15, 2026
Last Updated
April 13, 2026
Record last verified: 2026-04