Ignite Creation Date:
2024-07-17 @ 10:45 AM
Last Modification Date:
2024-10-26 @ 3:33 PM
Study NCT ID:
NCT06481761
Status:
RECRUITING
Last Update Posted:
2024-07-03
First Post:
2024-06-24
Brief Title:
The Effectiveness of Double-slot Brackets Versus Single-slot Brackets on the Rate of Canine Retraction
Sponsor:
Cairo University
Organization:
Cairo University
Study Overview
Official Title:
The Effectiveness of Double-slot Brackets Versus Single-slot Brackets on the Rate of Canine Retraction A Randomized Clinical Trial
Status:
RECRUITING
Status Verified Date:
2024-06
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
The aim of this Randomized clinical trial is to compare the efficacy of the double slot brackets compared to single slot-brackets in producing a controlled rate of upper canine retraction into premolar extraction space
patients will be randomly divided into one of the two groups CBCT cone beam computed tomography and dental models will be taken for each patient Pre-retraction and following the study completion
The rate of retraction will be evaluated for both groups as well as Amount of canine root movement and molar anchorage loss will be also assessed
patients will be randomly divided into one of the two groups CBCT cone beam computed tomography and dental models will be taken for each patient Pre-retraction and following the study completion
The rate of retraction will be evaluated for both groups as well as Amount of canine root movement and molar anchorage loss will be also assessed
Detailed Description:
Eligible patients will be examined for fulfilling the inclusion criteria All the recruited patients need extraction of upper first premolars followed by canine retraction with maximum anchorage
The patients will be randomly allocated to one of the two groups either Double slot brackets or single slot-brackets group
In Double slot bracket group Canine retraction will be made on two 0016 StSt stainless steel round wires each in one of the slots of the double slot brackets while in single slot-bracket group Retraction will be made on one 00170025 rectangular StSt arch wire
The patients will be seen on a monthly basis for follow up visit for reactivation of retraction to maintain constant force during the study An impression will be taken for the patients every visit fabricated dental models will be digitally scanned The scanned models will be used to monitor the rate of canine retraction
Every patient will be asked to take a CBCT image of the upper arch pre Retraction and after the completion of study duration 3 months After data collection assessors will carry on the measurements blindly Statistical analysis of the data will be done and the results will be compared to evaluate the effectiveness of both techniques for canine retraction
The patients will be randomly allocated to one of the two groups either Double slot brackets or single slot-brackets group
In Double slot bracket group Canine retraction will be made on two 0016 StSt stainless steel round wires each in one of the slots of the double slot brackets while in single slot-bracket group Retraction will be made on one 00170025 rectangular StSt arch wire
The patients will be seen on a monthly basis for follow up visit for reactivation of retraction to maintain constant force during the study An impression will be taken for the patients every visit fabricated dental models will be digitally scanned The scanned models will be used to monitor the rate of canine retraction
Every patient will be asked to take a CBCT image of the upper arch pre Retraction and after the completion of study duration 3 months After data collection assessors will carry on the measurements blindly Statistical analysis of the data will be done and the results will be compared to evaluate the effectiveness of both techniques for canine retraction
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None