Clinical Performance of Self-cured Universal Adhesive for Restoring Cervical Lesions in Geriatric Patients
Not Applicable
- Conditions
- Universal Adhesive
- Interventions
- Other: universal adhesive
- Registration Number
- NCT05054673
- Lead Sponsor
- Cairo University
- 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.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- UNKNOWN
- Sex
- All
- Target Recruitment
- 28
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
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description intervention universal adhesive PALFIQUE universal adhesive (Tokuyama self-cure universal adhesive) control universal adhesive 3M™ ESPE™ single bond Universal Adhesive
- Primary Outcome Measures
Name Time Method Measuring the Marginal adaptation 1 year modified USPHS criteria, ordinal
- Secondary Outcome Measures
Name Time Method Level of Marginal discoloration 1 year ordinal, modified USPHS criteria
level of Retention 1 year binary , modified USPHS criteria
level of Postoperative sensitivity 1 year binary , modified USPHS criteria
Rate of Secondary caries 1 year binary , modified USPHS criteria