Clinical Performance of Low Technique Sensitive Self Cured Universal Adhesive Vrs Light Cured Universal Adhesive in Patients With (NCCLs): 18 m RCT

NCT ID: NCT04572386

Last Updated: 2020-10-01

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

28 participants

Study Classification

INTERVENTIONAL

Study Start Date

2020-10-31

Study Completion Date

2022-07-31

Brief Summary

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

This study will be conducted to evaluate the clinical performance of self-cured adhesive versus light cured universal adhesive in non-carious cervical lesions (NCCL) resin composite restorations after 18 month

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.

Non Carious Cervical Lesion

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

TREATMENT

Blinding Strategy

NONE

Study Groups

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

Light cure universal bond

light cured 3m single bond universal

Group Type ACTIVE_COMPARATOR

light cure 3m single bond universal bond

Intervention Type OTHER

light -cure universal bond

self cure universal bond

self-cure universal bond (Palfique, Tokuyama, Japan)

Group Type ACTIVE_COMPARATOR

Self-cure universal bond (Palfique, Tokuyama, Japan)

Intervention Type OTHER

Self-cure universal bond with no light cure

Interventions

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

light cure 3m single bond universal bond

light -cure universal bond

Intervention Type OTHER

Self-cure universal bond (Palfique, Tokuyama, Japan)

Self-cure universal bond with no light cure

Intervention Type OTHER

Eligibility Criteria

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

Inclusion Criteria

* particepant with age rang 18-55
* particepant with non carious cervical lesion

Exclusion Criteria

* particepant outside age rang
* particepant with periodontal problem that might affect the teeth to be treated
Minimum Eligible Age

18 Years

Maximum Eligible Age

55 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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

Aya Gamal ashour

OTHER

Sponsor Role lead

Responsible Party

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

Aya Gamal ashour

principle investigator

Responsibility Role SPONSOR_INVESTIGATOR

Central Contacts

Reach out to these primary contacts for questions about participation or study logistics.

Aya Gamal, masters

Role: CONTACT

01004222615

Rawda husien, Phd

Role: CONTACT

01001097200

Other Identifiers

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

gsda.1986.2

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.