ClinicalTrials.Veeva

Menu

Remineralization of Early Carious Lesion Using Natural Agents Versus Bioadhesive Polymers

A

Al-Azhar University

Status

Completed

Conditions

Dental Caries

Treatments

Other: Carbopol
Other: Clove water extract
Other: Carboxymethyle cellulose

Study type

Interventional

Funder types

Other

Identifiers

NCT04390256
REC17-030

Details and patient eligibility

About

This study will be conducted to evaluate:

  1. The remineralization potential of natural agents (egg shell powder and clove extract) versus bioadhesive polymers (carbopol and carboxymethyl cellulose) with or without PH cycling using microhardness test.
  2. The clinical efficacy of all agents in patients with early carious lesions.

Enrollment

60 patients

Sex

All

Ages

18 to 30 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

    1. Criteria related to patient:

    • Age's eligible for trial was 18- 30 years.
    • Patient able to read and sign the informed consent form.
    • Cooperative patient who are willing to participate and able to continue the schedule time of wok keep good oral hygiene throughout the study.
    • Healthy volunteers.
    • Patient with moderate and high caries index. 2. Criteria related to tooth:
    • Patient with at least 2 white lesions (WSL) detected clinically on the buccal surface of permanent anterior teeth, one on each side. WSL selected either due to caries or orthodontic treatment (just following deboning).
    • Teeth with score1, 2, 3 according to ICDAS II.
    • Absence of preoperative pain, no mobility & tenderness on percussion.
    • Radiographically, the pre-operative inclusion criteria were absence of internal or external resorption, no periapical radiolucencies and no widening of periodontal ligament space..

Exclusion criteria

    1. Criteria related to patient:

    • Patient with Rampant uncontrolled caries.
    • Patient with compromised medical history.
    • Pregnant or breast feeding females.
    • Heavy smoker.
    • Patient who currently received extensive fluoride regiments for treatment of WSL.
    • Patients who planned to move within 3 months of enrollment.
    • Patient with evidence of xerostomia. 2. Criteria related to tooth:
    • Teeth with score 4, 5 according to ICDAS II.
    • Teeth with periapical pathology, internal or external resorption or exhibiting any symptoms of pulp pathology.
    • Teeth with questionable vitality or have root canal therapy.
    • Teeth have been pulp capped.
    • Teeth with periodontal pocket and bleeding on probing.
    • Cracked teeth.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

60 participants in 4 patient groups

Egg shell powder nanoparticles
Active Comparator group
Treatment:
Other: Carbopol
Other: Clove water extract
Other: Carboxymethyle cellulose
Clove water extract
Experimental group
Treatment:
Other: Carbopol
Other: Clove water extract
Other: Carboxymethyle cellulose
Carbopol
Experimental group
Treatment:
Other: Carbopol
Other: Clove water extract
Other: Carboxymethyle cellulose
Carboxymethyle cellulose
Experimental group
Treatment:
Other: Carbopol
Other: Clove water extract
Other: Carboxymethyle cellulose

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems