NCT07617480

Brief Summary

The goal of this clinical trial is to assess if sandblasting before acid etching reduce orthodontic bracket bond failure in fixed orthodontic treatment. The main question it aims to answer is:

  • What are the differences in bracket bond failure rate between acid etching with or without sandblasting method for the preparation of enamel? Researchers will compare acid etching with sandblasting method to acid etching without sandblasting method for enamel preparation to see if sandblasting prior to acid etching reduce bracket bond failure rate. Participants will:
  • Receive sandblasting of enamel before acid etching on one side of the mouth and only acid etching on the contralateral side for enamel preparation.
  • Participants would visit at the the OPD of Hospital at 3 weeks interval for follow up and for a total duration of 4 months to assess the changes. The number of bracket bond dislodgements at each session will be recorded .

Trial Health

75
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
15

participants targeted

Target at below P25 for not_applicable

Timeline
2mo left

Started Mar 2026

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
enrolling by invitation

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress58%
Mar 2026Sep 2026

Study Start

First participant enrolled

March 1, 2026

Completed
3 months until next milestone

First Submitted

Initial submission to the registry

May 18, 2026

Completed
14 days until next milestone

First Posted

Study publicly available on registry

June 1, 2026

Completed
1 month until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 1, 2026

Expected
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

September 1, 2026

Last Updated

June 1, 2026

Status Verified

May 1, 2026

Enrollment Period

4 months

First QC Date

May 18, 2026

Last Update Submit

May 24, 2026

Conditions

Keywords

Acid etchingSandblastingOrthodontic bracketEnamel preparationBond failure

Outcome Measures

Primary Outcomes (1)

  • To compare the bracket bond failure rate using acid etching with or without sandblasting method for the preparation of enamel.

    6 months

Study Arms (2)

Sandblasting

ACTIVE COMPARATOR

Sandblasting will be applied onto the vestibular surfaces of the teeth before applying the etchant

Procedure: Sandblasting with acid etching vs Acid etching alone

Acid Etching Alone

ACTIVE COMPARATOR

Only acid etching will be applied onto the vestibular surfaces of the teeth for enamel preparation.

Procedure: Acid Etching only

Interventions

Sandblasting will be applied onto the vestibular surfaces of the teeth before applying the etchant;

Sandblasting

Acid etching will be applied onto the vestibular surfaces of the teeth for enamel preparation.

Acid Etching Alone

Eligibility Criteria

Age18 Years - 64 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • Participants with good general health condition and oral hygiene status.
  • Age range of the patients will be 18 years and above.
  • Sex of the participants will be both male and female.
  • Patients with full permanent dentition present (excluding 3rd molar).
  • Patients with enamel integrity, absence of traumatic or carious lesion.
  • Participants who had no enamel pretreatment procedure performed with chemical agents.
  • Participants with no crossbite, scissor bite or occlusal interference (to prevent any potential early bond failure).

You may not qualify if:

  • Patients who have congenital enamel defects,
  • Patients who are in need of orthognathic surgery.
  • Patients with craniofacial syndromes.
  • Patients who present with partially erupted teeth with hypoplasia.
  • Patients for whom a rapid expander or a fixed functional appliance will be planned.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Bangladesh Medical University

Dhaka, 1000, Bangladesh

Location

Study Officials

  • Mahmood Sajedeen, BDS, FCPS

    Bangladesh Medical University

    STUDY DIRECTOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
PARALLEL
Model Details: Split mouth design.
Sponsor Type
OTHER
Responsible Party
SPONSOR INVESTIGATOR
PI Title
Associate Professor

Study Record Dates

First Submitted

May 18, 2026

First Posted

June 1, 2026

Study Start

March 1, 2026

Primary Completion (Estimated)

July 1, 2026

Study Completion (Estimated)

September 1, 2026

Last Updated

June 1, 2026

Record last verified: 2026-05

Data Sharing

IPD Sharing
Will not share

Confidentiality and privacy will be preserved by utilizing unique identifying codes instead of personal identifiers

Locations