MedDataX Logo

Chairside Time and Bond Failure of Non Custom Versus Custom Base Orthodontic Attachments During Indirect Bonding

NCT ID: NCT03365232

Last Updated: 2017-12-07

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

10 participants

Study Classification

INTERVENTIONAL

Study Start Date

2018-01-31

Study Completion Date

2019-03-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

compare the chair side time, clinical orthodontic attachment bond failure and accuracy of transfer between non custom attachment base and custom attachment base indirect techniques.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Orthodontic Appliance Complication

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

OTHER

Blinding Strategy

DOUBLE

Participants Outcome Assessors

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

non custom base attachment

Group Type EXPERIMENTAL

non custom base attachment

Intervention Type DEVICE

non custom base attachment

custom base attachment

Group Type ACTIVE_COMPARATOR

custom base attachment

Intervention Type DEVICE

custom base attachment

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

non custom base attachment

non custom base attachment

Intervention Type DEVICE

custom base attachment

custom base attachment

Intervention Type DEVICE

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

\- Patients should have

1. Maxillary sound teeth and undergoing fixed orthodontic treatment.
2. Space problems ranging from spacing to mild crowding.
3. Good oral hygiene.

Exclusion Criteria

1. Patients with partially erupted teeth in the maxillary arch .
2. Signs of caries, large restorations fluorosis, hypoplasia or abnormalities of crown morphology.
3. The need of banding.
4. Bad oral hygiene measures.
Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Cairo University

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Mohamed Saied Mahmoud Hassan

Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

CEBC-CU-2017-11-13

Identifier Type: -

Identifier Source: org_study_id