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Clinical Performance of Self-cured Universal Adhesive for Restoring Cervical Lesions in Geriatric Patients

Cairo University (CU) logo

Cairo University (CU)

Status

Unknown

Conditions

Universal Adhesive

Treatments

Other: universal adhesive

Study type

Interventional

Funder types

Other

Identifiers

NCT05054673
palfique bond

Details and patient eligibility

About

the study is conducted to evaluate the clinical performance of PALFIQUE universal adhesive (Tokuyama self-cure universal adhesive), Versus 3m ESPE™ single bond Universal Adhesive, for restoring cervical lesions in geriatric patients over one year.

Enrollment

28 estimated patients

Sex

All

Ages

60+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • The patient had to be in good general health
  • Geriatric patients
  • Have an acceptable oral hygiene level
  • Class V cavities in anterior and posterior teeth
  • Males & females included
  • Anticipated availability for recalls (6 months and 12 months) through the 1-year study period

Exclusion criteria

  • Lack of written informed consent to participate
  • Poor oral hygiene,
  • Severe bruxism
  • Severe or chronic periodontitis
  • Allergies to components of the materials used
  • Underage patients
  • Non vital pulp

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

28 participants in 2 patient groups

intervention
Experimental group
Description:
PALFIQUE universal adhesive (Tokuyama self-cure universal adhesive)
Treatment:
Other: universal adhesive
Other: universal adhesive
control
Active Comparator group
Description:
3M™ ESPE™ single bond Universal Adhesive
Treatment:
Other: universal adhesive
Other: universal adhesive

Trial contacts and locations

0

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Central trial contact

Maysaa M Mostafa, B.D.S.

Data sourced from clinicaltrials.gov

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