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 @ 7:51 PM
Ignite Modification Date:
2025-12-24 @ 7:51 PM
NCT ID:
NCT02771704
Eligibility Criteria:
Inclusion Criteria:
* Patient should be able to give informed consent.
* had at least 5 teeth with moderate size caries lesions (for 5 treatments), to be exact with the lesion size.
* the carious lesion should at least penetrate to the inner ½ of dentine thickness.
* the lesion should be suitable for the placement of a Vitrabond lining of 0.5-1.0 mm
* permanent restoration should be a part of a current and approved treatment plan
Exclusion Criteria:
* Inability of the patient to give informed consent.
* teeth had received temporary restoration
* isolation with rubber dam is not possible.
* if cavity preparation was contaminated due to gingival bleeding
All patients were placed under a follow up system for the purpose of addressing any complaints that might result from the sampling procedure.
Healthy Volunteers:
False
Sex:
ALL
Study:
NCT02771704
Study Brief:
Protocol Section:
NCT02771704