Universal Adhesive
Conditions
Brief summary
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.
Interventions
OTHERuniversal adhesive
PALFIQUE universal adhesive
Sponsors
Cairo University
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)
Masking description
Triple (Participant, Investigator, Outcomes assessor)
Intervention model description
parallel assignment
Eligibility
Sex/Gender
ALL
Age
60 Years to No maximum
Healthy volunteers
Yes
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
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Measuring the Marginal adaptation | 1 year | modified USPHS criteria, ordinal |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| level of Retention | 1 year | binary , modified USPHS criteria |
| Level of Marginal discoloration | 1 year | ordinal, modified USPHS criteria |
| Rate of Secondary caries | 1 year | binary , modified USPHS criteria |
| level of Postoperative sensitivity | 1 year | binary , modified USPHS criteria |
Contacts
Primary ContactMaysaa M Mostafa, B.D.S.
Outcome results
None listed