Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 11:50 AM
Ignite Modification Date:
2025-12-24 @ 11:50 AM
NCT ID:
NCT05466461
Eligibility Criteria:
Inclusion Criteria:
* ages 18 to 55 years.
* Male or female patients.
* Patients with no history of allergic reactions to methacrylate compounds and in good general health.
* Patients with good general health.
* Patients with good recall availability. Patients required Class V restoration
* Vital teeth with normal appearance and morphology.
* Absence of clinical symptoms of irreversible pulpitis, such as spontaneous pain or sensitivity to pressure.
* Absence of clinical diagnosis of pulp exposure, fistula, swelling of periodontal tissues, and/or abnormal tooth mobility .
* No defects and lesions for other operative intervention, occlusal and proximal contacts with adjacent teeth.
Exclusion Criteria:
* Patients with history of any adverse reaction to clinical materials of the types to be used in the evaluation.
* Pregnant and lactating females.
* Any patients with medical and/or dental histories which could possibly complicate the provision of the proposed restoration and/or influence behavior and performance of the restorations in clinical service.
* They are included in the evaluation of other restorative materials and systems involving the anterior and/or posterior teeth.
* Patients who maintain an unacceptable standard of oral hygiene.
* Teeth with noncarious cervical lesions.
* Severe tooth sensitivity.
* Non-vital or fracture or cracked teeth.
* Tooth with defective restoration.
* Teeth with advanced periodontal diseases.
* There is evidence occlusal parafunctions and/or atypical tooth wear.
Healthy Volunteers:
True
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
55 Years
Study:
NCT05466461
Study Brief:
Protocol Section:
NCT05466461