Bond Strength Evaluation

NCT ID: NCT07196618

Last Updated: 2025-12-18

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

ACTIVE_NOT_RECRUITING

Clinical Phase

NA

Total Enrollment

30 participants

Study Classification

INTERVENTIONAL

Study Start Date

2025-09-01

Study Completion Date

2026-03-31

Brief Summary

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

This study was evaluated the effect of dimethyl sulfoxide pretreatment on tensile bond strength and nanoleakage of resin composite bonded to aged dentin.

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.

Bonding

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

PREVENTION

Blinding Strategy

SINGLE

Participants

Study Groups

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

DMSO

Group Type ACTIVE_COMPARATOR

dimethyl sulfoxide

Intervention Type DRUG

dentin pretreated using dimethyl sulfoxide and follow up of patients at 2 weeks, 3 months and 6 months

CHX

Group Type ACTIVE_COMPARATOR

Cholorhexidine

Intervention Type DRUG

dentin pretreated using chlorhexidine and follow up of patients at 2 weeks, 3months and 6 months

Interventions

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

dimethyl sulfoxide

dentin pretreated using dimethyl sulfoxide and follow up of patients at 2 weeks, 3 months and 6 months

Intervention Type DRUG

Cholorhexidine

dentin pretreated using chlorhexidine and follow up of patients at 2 weeks, 3months and 6 months

Intervention Type DRUG

Eligibility Criteria

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

Inclusion Criteria

* Patients included in the study will be required to present at least one of non caries cervical lesion with sclerotic dentin without pulpal involvement.
* Age of patient: 50 - 75 years
* Patients with non caries cervical lesion will be standardized by clinical performance (FDI world dental federation).

Exclusion Criteria

* Teeth with deep dentinal lesions with pulpal involvement, abscess, pain or swelling
* Developmental disorders and adjacent soft tissue lesions
* Patients with systemic illness will be excluded.
Minimum Eligible Age

50 Years

Maximum Eligible Age

75 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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

Al-Azhar University

OTHER

Sponsor Role lead

Responsible Party

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

Aisha Nasr Ali Zahran

Doctor

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Aisha Zahran

Role: STUDY_DIRECTOR

Al-Azhar University

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Al-Azhar university

Cairo, , Egypt

Site Status

Countries

Review the countries where the study has at least one active or historical site.

Egypt

Other Identifiers

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

P-OP-23-03

Identifier Type: -

Identifier Source: org_study_id