Ignite Creation Date:
2024-10-26 @ 3:37 PM
Last Modification Date:
2024-10-26 @ 3:37 PM
Study NCT ID:
NCT06554769
Status:
COMPLETED
Last Update Posted:
None
First Post:
2024-02-07
Brief Title:
Efficiency of Rigid Versus Non-rigid Indirect Anchorage During Canine Retraction A Split Mouth Randomized Study
Sponsor:
None
Organization:
None
Study Overview
Official Title:
Efficiency of Rigid Versus Non-rigid Indirect Anchorage During Canine Retraction A Split Mouth Randomized Study
Status:
COMPLETED
Status Verified Date:
2024-08
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
No
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
Indirect anchorage In-A has been broadly used for anchorage reinforcement during anterior segment retraction The study compared between the efficacy of rigid vs non-rigid connections of In-A i during upper canine retraction in dentoalveolar protrusion cases
Detailed Description:
Fifteen female patients with dentoalveolar protrusion were included in this study A miniscrew was inserted following levelling and alignment between the upper first molar and second premolar of both sides Randomization was applied before first premolar extraction where one side of the arch received a rigid indirect anchorage connection Group I of 0019 x 0025-inch stainless steel StSt archwire from the miniscrew to the auxiliary tube of the upper first molar band and the other side received a non-rigid indirect anchorage connection Group II of 0014-inch StSt ligature ligating the upper second premolar to the miniscrew Canine retraction was performed on 0017 x 0025-inch StSt archwire applying 15 N retraction force The duration of the study was 7 months Data was collected from digitized models where anchorage loss of the upper first molar relative to the frontal plane and the vertical position of the upper second premolar were measured
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None