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:
2025-12-25 @ 4:18 AM
Ignite Modification Date:
2025-12-25 @ 4:18 AM
NCT ID:
NCT03530020
Eligibility Criteria:
Inclusion Criteria:
* All subjects are required to be:
1. Age range of the patients from 21-50 years old; able to read and sign the informed consent document, illiterate patient will be avoided.
2. Patients able physically and psychologically to tolerate conventional restorative procedures.
3. Patients with no active periodontal or pulpal diseases, having teeth with good restorations.
4. Patients with teeth problems indicated for full coverage restoration (e.g. moderate to severe discoloration, coronal fracture where partial coverage would lack retention, malposed or malformed teeth).
5. Patients with root canal treated teeth requiring full coverage restorations.
6. Presence of an opposing natural tooth which is non-restored or minimally restored. (Minimally restored is defined as teeth which have no restoration greater than a Class II a restoration)
7. The opposing arch doesn't have a full coverage restoration or a partial denture.
8. Patients willing to return for follow-up examinations and evaluation.
Exclusion Criteria:
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1. Patients with poor oral hygiene.
2. Patients with psychiatric problems or unrealistic expectation (patient that has phobia from dental treatments or needle bunch).
3. Patients have no opposite occluding dentition in the area intended for restoration
4. Patients suffer from Para functional habits or temporomandibular disorders. (as those patient may have wear which will affect the results)
Healthy Volunteers:
True
Sex:
ALL
Minimum Age:
21 Years
Maximum Age:
50 Years
Study:
NCT03530020
Study Brief:
Protocol Section:
NCT03530020