"Comparative Evaluation of 3 Dimensional Changes of Dentition in Post Orthodontic Patients With Immediate vs Delayed (Post 24 Hours) Retainer Delivery
Relapse
About this trial
This is an interventional prevention trial for Relapse focused on measuring Orthodontic Retention
Eligibility Criteria
Inclusion Criteria: Adult orthodontic patients treated with 022*028 MBT appliance with following sequence of wires- 014, 016, 16*22, 17*25, 19*25 NiTi followed by 19*25 SS. Treatment duration of 24-36 months with Optimal functional occlusion at end of treatment (PAR score >70%). Class I bimax and Class II div I with pre-treatment Little's irregularity index <6mm in both upper and lower arch. Nonsurgical and non-orthopedic patients. Non syndromic patients and no impaction of teeth except third molars. No previous orthodontic treatment. Optimal periodontal condition and Good oral hygiene. Good compliance regarding retainer wear (Cases who never missed more than 2 consecutive appointment and who reported with less no of breakages) Exclusion Criteria: Subjects with incomplete orthodontic treatment. TMJ disorder patients. Any systemic disease affecting bone and general growth. Patients with incomplete records. Patient who fail to follow up or undergo complete treatment. Patient with learning difficulties
Sites / Locations
- Post Graduate Institute of Dental SciencesRecruiting
Arms of the Study
Arm 1
Arm 2
Other
Active Comparator
control group- immediate retainer delivery
experimental group- delayed retainer delivery
Retainer will be given to the patients immediately [ Just after debonding]
Retainer will be given to the patient 24 hours post debonding.