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 @ 3:00 PM
Ignite Modification Date:
2025-12-24 @ 3:00 PM
NCT ID:
NCT05585359
Eligibility Criteria:
Inclusion Criteria: Patients were enrolled to the present study if they fulfilled the inclusion criteria of being fit and healthy (ASA I and II).
* Adults with an age range of 18-45 years old, with no sex predication.
* Patients diagnosed with pulp necrosis in mature maxillary or mandibular anterior teeth with negative response to both cold and electrical pulp testing.
* Associated with or without swelling /sinus tract.
* Has radiographic evidence of periapical radiolucency
Exclusion Criteria: Patients with medically compromised conditions (ASA III and IV).
* Patients who are allergic to the drugs or pharmaceuticals used in the trial (mainly ciprofloxacin or metronidazole).
* Patients with presence of periodontal pockets, pathological mobility, ankyloses, root fracture.
* Patients with non-restorable teeth, teeth with pulp space needed for post cementation.
* Teeth with previous root canal treatment, teeth with developmental anomalies, and teeth with external or internal resorption.
Healthy Volunteers:
True
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
45 Years
Study:
NCT05585359
Study Brief:
Protocol Section:
NCT05585359