ClinicalTrials.gg
CompletedNCT07503314SLBs CBs RCTUpdated Mar 31, 2026

Comparison of Alignment Efficiency, Arch Dimensional Changes, and Passive Extraction Space Closure Between Self-Ligating and Conventional Brackets

An interventional study of Self-Ligating Brackets (SLB) and Conventional Bracket in Dental Crowding, Passive Extraction Space and Intercanine Width, sponsored by Saidu College of Dentistry. Completed at 1 site in Pakistan. Open to participants aged 13 Years to 30 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-03-31.

Sponsored by Saidu College of Dentistry · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Registered 2 years 1 month after the study started (first participant enrolled Feb 2024, registered Mar 2026).
Phase
Not applicable
Study type
Interventional
Enrollment
70
Allocation
Randomized
Ages
13 Years to 30 Years
Sex
All
01

Study summary

Purpose:

This study aims to compare two types of orthodontic braces - self-ligating brackets (SLBs) and conventional brackets (CBs) - to see which one aligns teeth faster, affects the width of the dental arch, and closes spaces after premolar extractions more efficiently.

Who Can Join:

Ages 13-30 years Moderate to severe dental crowding Skeletal Class I or mild to moderate Class II malocclusions Good oral hygiene Requiring extraction of premolars

What Participants Will Do:

Participants are randomly assigned to either the SLB group or the CB group. Braces are bonded to the teeth following standard orthodontic procedures. Dental impressions and measurements will be taken at baseline, 3, 6, and 9 months.

No extra devices (like power chains) will be used for space closure during the study.

What is Being Measured:

Alignment of teeth using Little's Irregularity Index Intercanine and intermolar widths (arch dimensions) Passive closure of extraction spaces

Why This Study is Being Done:

The study investigates whether SLBs provide any clinical advantage over conventional braces in terms of faster alignment, arch width changes, and efficient space closure in extraction cases. This could help orthodontists make evidence-based decisions when choosing braces.

Study Duration:

Total observation period: 9 months Monthly follow-ups for adjustments and measurements

Read the detailed description

This prospective, randomized controlled trial was conducted to evaluate the clinical effects of self-ligating brackets (SLBs) versus conventional brackets (CBs) in patients requiring premolar extractions. The study included 70 participants aged 13-30 years with moderate to severe crowding and skeletal Class I or mild-to-moderate Class II malocclusions.

Participants were randomly assigned to either the SLB or CB group (35 participants each) using computer-generated random numbers and allocation concealment through sequentially numbered, opaque, sealed envelopes. Blinding of the operator and participants was not possible due to the nature of the interventions; however, outcome assessors were blinded by covering brackets on dental casts with beading wax.

The study assessed alignment efficiency, arch dimensional changes, and passive extraction space closure over a 9-month period. Dental impressions and study casts were collected at baseline, 3, 6, and 9 months. Alignment was quantified using Little's Irregularity Index, while intercanine and intermolar widths and passive extraction space closure were measured using digital calipers. No active space-closing auxiliaries, such as power chains or springs, were used during the observation period.

All treatments were performed by trained orthodontic residents with calibration to ensure consistency in bonding procedures, archwire sequence, and ligation methods. Linear mixed-effects models with repeated measures and covariates (age, gender, and malocclusion type) were used for statistical analysis, and regression coefficients with 95% confidence intervals were reported.

The trial aims to determine whether SLBs differ from conventional brackets in terms of alignment speed, arch dimensional changes, and passive space closure in extraction cases. Findings from this study can inform evidence-based bracket selection and clinical decision-making in orthodontic practice.

02

Conditions studied

  • Dental Crowding
  • Passive Extraction Space
  • Intercanine Width
  • Intermolar Width

Browse trials for

Keywords

  • Self-ligating brackets
  • Conventional brackets
  • Orthodontic alignment
  • Dental crowding
03

In context

Crowding

88 studies on the registry are indexed under Crowding; 22 are open to participants now.

This study's enrollment of 70 is above the median of 36 across 74 interventional studies indexed under Crowding.

Browse Crowding studies →

Lead sponsor

Saidu College of Dentistry is the lead sponsor of 4 studies on the registry; 3 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
13 Years to 30 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Eligibility criteria

Inclusion Criteria Age 13-30 years, any gender Moderate (4-8 mm) or severe (>8 mm) dental crowding Skeletal Class I (ANB 0-20) or mild-to-moderate Class II (ANB 3-50) Normal or vertical growth pattern (FMA 22-280) Good oral hygiene (plaque index ≤1) Require extraction-based orthodontic treatment

Exclusion Criteria Previous orthodontic treatment Asymmetric extractions Systemic diseases or medications affecting bone metabolism Cleft lip/palate or other craniofacial anomalies Congenital absence of teeth (except third molars) Low-angle (hypodivergent) growth pattern Inability to comply with treatment/follow-up

05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
70 participants (actual)

Study arms

  • Active comparator
    Conventional Bracket Group (CB)

    Participants in this group received 0.022-inch slot conventional MBT brackets (Dentaurum, Germany) bonded to all teeth up to the second premolars. Alignment started with 0.014-inch NiTi archwires and progressed according to a standardized archwire sequence. Stainless steel lacebacks were used for early canine control, and no active space-closing auxiliaries (e.g., power chains or closed-coil springs) were applied during the 9-month observation period. Outcome measurements were taken at baseline, 3, 6, and 9 months on blinded study casts.

    Device: Self-Ligating Brackets (SLB)

  • Experimental
    Self-Ligating Bracket Group (SLB)

    Participants in this group received 0.022-inch slot self-ligating MBT brackets (American Orthodontics, USA) bonded to all teeth up to the second premolars. Alignment started with 0.014-inch NiTi archwires and progressed using the same standardized archwire sequence. Stainless steel lacebacks were applied for early canine control, and no active space-closing auxiliaries were used during the 9-month observation period. Outcome measurements were taken at baseline, 3, 6, and 9 months on blinded study casts.

    Device: Conventional Bracket

Interventions

  • DeviceSelf-Ligating Brackets (SLB)

    Participants received 0.022-inch slot MBT conventional brackets (Equilibrium 2, Dentaurum, Germany) bonded to all teeth up to the second premolars. Alignment began with 0.014-inch NiTi archwires and progressed through the same standardized sequence as the SLB group. Stainless steel lacebacks were applied for early canine control. No active space-closing auxiliaries (power chains or closed-coil springs) were used during the 9-month observation period. Outcome measurements were taken at baseline, 3, 6, and 9 months on blinded study casts.

  • DeviceConventional Bracket

    Participants in this arm received 0.022-inch slot MBT conventional brackets (Equilibrium 2, Dentaurum, Germany) bonded to all teeth up to the second premolars. Alignment began with 0.014-inch NiTi archwires and progressed using a standardized archwire sequence (0.016, 0.018 NiTi, 0.016×0.022 NiTi, 0.019×0.025 stainless steel). Stainless steel lacebacks were applied for early canine control, and no active space-closing auxiliaries (e.g., power chains or NiTi closed-coil springs) were used during the 9-month observation period. Outcome measurements were taken at baseline, 3, 6, and 9 months on blinded study casts.

06

What researchers measure

Primary outcomes

  1. Dental alignment assessed by Little's Irregularity Index

    The primary outcome is the degree of dental alignment in extraction cases, measured on study casts using Little's Irregularity Index. Measurements were performed by a single calibrated examiner blinded to bracket type using a digital caliper (0.01 mm accuracy). Higher scores indicate greater crowding, while lower scores indicate improved alignment.

    Time frame: Baseline (T₀) to 9 months (T₃), assessed at 3-month intervals

  2. Intermolar width

    The primary outcome is the degree of dental alignment in extraction cases, measured on study casts using Little's Irregularity Index. Measurements were performed by a single calibrated examiner blinded to bracket type using a digital caliper (0.01 mm accuracy). Higher scores indicate greater crowding, while lower scores indicate improved alignment.

    Time frame: Baseline (T₀) to 9 months (T₃), assessed at 3-month intervals

Secondary outcomes

  1. Intercanine width

    Distance between the cusp tips of the canines on study casts. Measured by a blinded examiner using a digital caliper (0.01 mm accuracy) to monitor transverse changes in the anterior arch.

    Time frame: Baseline (T₀) to 9 months (T₃), assessed at 3-month intervals

  2. Passive extraction space closure

    Measured at extraction sites as the distance between nearest reproducible points on crowns adjacent to extraction sites. No active space-closing auxiliaries were used to isolate the effect of bracket type. Measured by a blinded examiner using digital calipers.

    Time frame: Baseline (T₀) to 9 months (T₃), assessed at 3-month intervals

07

Study locations

1 site
  • Marium Jamil
    Lahore, Punjab Province 2500, Pakistan
08

References and documents

Publications

  • 14. Scott P, DiBiase AT, Sherriff M, Cobourne MT. Alignment efficiency of Damon3 self-ligating and conventional orthodontic bracket systems: a randomized clinical trial. American journal of orthodontics and dentofacial orthopedics. 2008;134(4):470. e1-. e8. 2. Fleming PS, DiBiase AT, Sarri G, Lee RT. Comparison of mandibular arch changes during alignment and leveling with 2 preadjusted edgewise appliances. American Journal of Orthodontics and Dentofacial Orthopedics. 2009;136(3):340-7. 3. Pandis N, Polychronopoulou A, Katsaros C, Eliades T. Comparative assessment of conventional and self-ligating appliances on the effect of mandibular intermolar distance in adolescent nonextraction patients: a single-center randomized controlled trial. American journal of orthodontics and dentofacial orthopedics. 2011;140(3):e99-e105.

Individual participant data

Plan to share: Yes — Individual participant data (IPD) will include de-identified demographic, clinical, and outcome measurements (Little's Irregularity Index, intercanine and intermolar widths, arch depth, passive extraction space) collected during the trial. No personal identifiers will be included. Supporting documents such as study protocol, statistical analysis plan, and analytic code will also be shared.

Supporting information: Statistical analysis plan, Analytic code

Time frame: IPD and supporting information will be available from 6 months after publication of the trial results and remain accessible for 5 years.

Access criteria: Qualified researchers can access the data for scientific purposes upon request. Requests require a brief proposal and agreement to data use terms to protect participant confidentiality. Data will be shared via secure email or repository upon request.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 31, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07503314
Lead sponsor
Saidu College of Dentistry
Responsible party
Dr Ajmal Khan (The University of Lahore, Pakistan, Saidu College of Dentistry) — Principal investigator
First posted
Mar 31, 2026
Start date
Feb 1, 2024
Primary completion
Jun 25, 2025
Completion
Jun 25, 2025
Last update
Mar 31, 2026

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Mar 2026. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion