- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06366737
En-mass Retraction by KILBON Versus CAT Appliances
September 16, 2024 updated by: Zeinab mohamed, Cairo University
Effectiveness Of Lingual Retractor Versus Clear Aligner Appliances In En-mass Retraction Of Maxillary Anterior Teeth Segment In Adult Patients: A Randomized Clinical Trial
en-mass retraction by lingual retractor versus clear alighner therapy
Study Overview
Status
Not yet recruiting
Conditions
Intervention / Treatment
Detailed Description
Comparative Effectiveness Of Lingual Retractor Versus Clear Aligner Appliances In Adult Patients With Maxillary Dentoalveolar Protrusion Treated By Upper First Premolars Extraction And Enmass Retraction Of Maxillary Anterior Teeth Segment Using Palatal Orthodontic Miniscrews :A Randomized Clinical Trial
Study Type
Interventional
Enrollment (Estimated)
30
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Cairo, Egypt
- Faculty of Dentistry
-
Contact:
- zainab abdulrhman
- Phone Number: 00201092445775
- Email: zeinab_mohammed@dentistry.cu.edu.eg
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- adult patients with maxillary dentoalveolar protrusion with mild crowding
Exclusion Criteria:
- - adult patients with maxillary dentoalveolar protrusion with moderate to severe crowding
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: KILBON appliance
en-mass retraction by lingual retractor
|
palatal TAD assissted lingual appliance for en-mass retraction
|
|
Active Comparator: CAT appliance
en-mass retraction by clear aligner
|
palatal TAD assissted clear aligner
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Patient satisfaction during & after phase I treatment.
Time Frame: 6 months
|
questionnaire
|
6 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
inclination of upper anterior teeth
Time Frame: 6 months
|
angle measurement of long axis of maxillary central to maxillary plane in degrees
|
6 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Estimated)
October 1, 2024
Primary Completion (Estimated)
June 1, 2025
Study Completion (Estimated)
August 1, 2025
Study Registration Dates
First Submitted
March 28, 2024
First Submitted That Met QC Criteria
April 10, 2024
First Posted (Actual)
April 16, 2024
Study Record Updates
Last Update Posted (Actual)
September 19, 2024
Last Update Submitted That Met QC Criteria
September 16, 2024
Last Verified
September 1, 2024
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- CEBD-CU-2024-03-02
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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