Acceleration of Tooth Movement Clinical Trial
Official title:
Mandibular Second Molar Protraction Assisted by and Piezocision
This study was conducted to compare the rate of second molar protraction, level of Interleukin1-β in gingival crevicular fluid, periodontal health (gingival index, plaque index, and periodontal pocket depth) and perception of pain in patients treated by molar protraction with piezocision vs control (no piezocision).
Twenty-six subjects (39 Molars) who presented with at least one extracted mandibular first
molar were selected to participate in the study. The subjects were subdivided into one of 3
groups as follows: group 1 consisted of 18 molars (13 molars from patients with bilateral
first molar extraction space and 5 molars from patients with unilateral first molar
extraction space) where piezocision was performed immediately before molar protraction; group
2 consisted of 21 molars (13 from patients with bilateral first molar extraction space and 8
molars from patients with unilateral first molar extraction space) where molar protraction
was performed with no piezocision; group 3 consisted of 21 molars (group 2 subjects where
piezocision was carried on after 3 months of molar protraction with no piezocision. After
reaching 0.019X0.025" SS arch wire, NiTi coil spring was used for space closure (protraction
force was 150g) attached from the lower second molar hook to the head of the mini-screw.
Piezocision was performed by making 2 vertical incisions mesial and distal to the extraction
space. Piezotome was inserted in the incisions previously made and bone cuts were done with a
length up to mucogingival line and depth of 3 mm.
Gingival crevicular fluid (GCF) sample was obtained from the mesiogingival side of the lower
second permanent molar with use of Periopaper. GCF sample was repeated 1 day, 1 week and 4
weeks after molar protraction with piezocision or with no piezocision. Pain was assessed
using visual analog scale (VAS). Patients were requested to report the level of pain for 7
consecutive days.
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Status | Clinical Trial | Phase | |
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Completed |
NCT02026258 -
Efficiency of Piezotome-Corticision Assisted Orthodontics
|
N/A |