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 @ 10:38 PM
Ignite Modification Date:
2025-12-24 @ 10:38 PM
NCT ID:
NCT01860235
Eligibility Criteria:
Inclusion Criteria:
* eligible individuals for the study were selected from those requiring SRP with at least 2 experimental teeth in four of the six sextants.
* each experimental teeth had to present ≥ 1 site with probing depth ≥ 5 mm associated with BP after treatment of gingivitis (without marginal bleeding).
* furthermore, individual should present ≥ 18 years-old, have not ever done periodontal treatment and be able to understand Verbal Scale (VS) and Visual Analog Scale (VAS).
Exclusion criteria:
* patients that related allergy history or sensitivity reaction to any used amide or ester anesthetics form,
* who received anesthesia or sedation 12 hours before SRP,
* who presented ulcerated lesions or abscesses in the oral cavity,
* who presented oral pathologies with immediate surgical,
* who had prior abuse alcohol history, pregnant women,
* who presented uncontrolled hypertension or
* who had participated in a clinical trial of investigational drug before four months from the beginning of this study.
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT01860235
Study Brief:
Protocol Section:
NCT01860235