← Back to all trials
Recruiting
NCT07585721
Postoperative Pain and Substance P Levels After Bioceramic vs Calcium Hydroxide Intracanal Medicaments in Symptomatic Apical Periodontitis
Conditions: Symptomatic Apical Periodontitis
Sex: All
Ages: 18 Years – 45 Years
Healthy volunteers: Yes
Phase: NA
Enrollment: 28
Sponsor: Future University in Egypt
Location: Future University in Egypt - Faculty of Oral and Dental Medicine Cairo
Summary
Clinical Evaluation of the Postoperative Pain and Substance P levels Following the use of Bioceramic verses Calcium Hydroxide Intracanal Medicaments in Permanent Mandibular molars with Symptomatic Apical Periodontitis
Eligibility Criteria
Inclusion Criteria:
* \- Patients aged 18-45 years with no sex predilection
* Medically free Patients with no systemic conditions that can affect post operative pain response.
* Patients should not be taking any pain medications 24 hours before intervention
* Positive patients' acceptance for participating in the study
* Patient able to sign informed consent
* Permanent mandibular molars diagnosis with Symptomatic Apical Periodontitis
* Permanent molars without any anatomical variations or severe curvatures
Exclusion Criteria:
* \- Medically compromised patients
* Patients who have received antibiotic therapy within the last 2 weeks.
* Pregnant or lactating women.
* Patients with known allergy to any of the irrigants used.
* Patients with swelling or acute peri-apical abscess or fistulous tract.
* Teeth that have:
* Wide or open apex .
* Vital pulp tissue .
* Periodontally affected with grade 2or 3 mobility.
* Non restorable teeth .
* Abnormal anatomy and calcified canals .
* Pervious root canal treatment.
* severe curved canal
* Buccolingual and mesiodistal radiographs were taken to evaluate the root canal anatomy
Source: ClinicalTrials.gov (NCT07585721). StuddyBuddy aggregates publicly available trial information.