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Comparison Of En-Masse Retraction With Two-Step Retraction Using Mini-Implant As Anchorage

Comparison Of En-Masse Retraction With Two-Step Retraction Using Mini-Implant As Anchorage - A Randomized Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05963438
Enrollment
80
Registered
2023-07-27
Start date
2022-10-10
Completion date
2024-06-04
Last updated
2025-09-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

En-masse Retraction to Two- Steps Retraction

Keywords

En-masse retraction, Two step retraction, mini-implant, anchorage

Brief summary

This Randomized Control Trial will be conducted to compare the effects of en-masse retraction to two- steps retraction on sagittal, vertical and dental dimensions using mini-implant as anchorage.

Detailed description

Extractions of teeth are the commonest approach in treating orthodontic problems. There is several extraction protocol commonly employed in the orthodontic correction of class II malocclusion ranging from the extraction of two premolars (20.2%) to four premolars (42.9%). Retraction of anterior teeth followed by the extraction of premolars requires anchorage to restrict the mesial movement of posterior teeth. Anchorage control is a major factor in achieving successful orthodontic treatment and it can be achieved by variety of appliances, of which titanium screws have been considered as an absolute source of anchorage in orthodontics treatment. The anchorage reinforced from mini-implant is helpful in minimizing anchorage loss and accepted heavy traction forces. Retraction of anterior teeth can be achieved either by en-masse retraction, moving all the six anterior teeth together in a single step or by two-step retraction, separately retract canines in first step followed by retracting the four anteriors in the second step. This Randomized Control Trial will be conducted to compare the effects of en-masse retraction to two- steps retraction on sagittal, vertical and dental dimensions using mini-implant as anchorage. 80 patients will be included in this study after meeting the eligibility criteria. Each group will contain 40 patients. The patients will be divided in two groups i.e. two-step retraction group (control group) and en-masse group (experimental group), through software generated randomization table. Two-step retraction group (control group) In this group, immediately after placement of mini-implant and extractions of upper first premolars, heavy ligation will be done from mini-implant to maxillary second premolar and first molar. Canine will be retracted by sliding mechanics and the four anterior teeth will be retracted by loop mechanics. Loops will be activated every three weeks by 1 mm. Retraction will be stopped when canines establish class I relationship and a good incisor relationship will be obtained in both the groups En-masse retraction group(experimental group) After placement of mini-implants and extraction of maxillary first premolar, rectangular stainless steel arch wire with anterior 8mm height crimpable hooks distal to the lateral incisors will be inserted and force will be applied using elastic chains attached between the mini-implant and the hooks for conducting en-masse retraction. Elastic chains will replace after every three weeks. Pretreatment lateral cepalogram will be taken at time of enrolment (T1) and post-treatment lateral cephalogram taken after 12 months of orthodontic treatment (T2). All cephalometric radiograph will be traced on acetate tracing sheets 0.5 μm in thickness using a sharp 4H pencil on a view box using transilluminated light in a dark room. The analysis will be done on pretreatment cephalogram (T1) and post treatment lateral cephalogram (T2) and then their measurements will be compared to find out changes in the sagittal, vertical and dental dimensions.

Interventions

PROCEDUREanterior retraction

After placement of mini-implants and extraction of maxillary first premolar, retraction of anterior either simultaneously or separately depending on the allocated group will be done

Sponsors

Dow University of Health Sciences
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to 25 Years
Healthy volunteers
Yes

Inclusion criteria

* 1\. Both male and female patients with age of 18- 25 years. 2. Cases treated with upper first premolars extractions. 3. Cases having class II molar relation which is mesiobuccal cusp of maxillary first permanent molar occludes anterior to the buccal groove of mandibular first molar on both sides as assessed clinically. 4\. Overjet \> 5mm and \< 12mm as assessed clinically. 5. Cases with no remaining growth as assessed by cervical vertebrae maturation stages (cvm) ≥4 on lateral cephalometric radiograph . 6\. Cases with no congenitally missing teeth (excluding third molars).

Exclusion criteria

* 1\. Long term use of systemic corticosteroids, calcium channel blockers & anti-inflammatory drugs. 2\. Cases with syndromes like cleft lip and palate as assessed clinically. 3. Cases in which active growth is still taking place as assessed by cervical vertebrae maturation stages (cvm) ≤ 3 on lateral cephalometric radiograph. 4\. Radiographic evidence of bone loss. 5. Periodontal disease as assessed clinically.

Design outcomes

Primary

MeasureTime frame
To compare sagittal, vertical and dental dimensions following en-masse retraction with two-step retraction using mini-implants as anchorage.Pretreatment lateral cepalogram will be taken at time of enrolment (T1) and post-treatment lateral cephalogram taken after 12 months of orthodontic treatment (T2).

Countries

Pakistan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026