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

A

Aya Gamal ashour

Status

Unknown

Conditions

Non Carious Cervical Lesion

Treatments

Other: Self-cure universal bond (Palfique, Tokuyama, Japan)
Other: light cure 3m single bond universal bond

Study type

Interventional

Funder types

Other

Identifiers

NCT04572386
gsda.1986.2

Details and patient eligibility

About

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

Enrollment

28 estimated patients

Sex

All

Ages

18 to 55 years old

Volunteers

No Healthy Volunteers

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

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

28 participants in 2 patient groups

Light cure universal bond
Active Comparator group
Description:
light cured 3m single bond universal
Treatment:
Other: light cure 3m single bond universal bond
self cure universal bond
Active Comparator group
Description:
self-cure universal bond (Palfique, Tokuyama, Japan)
Treatment:
Other: Self-cure universal bond (Palfique, Tokuyama, Japan)

Trial contacts and locations

0

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Central trial contact

Aya Gamal, masters; Rawda husien, Phd

Data sourced from clinicaltrials.gov

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