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Clinical Trials in Egypt / NCT07468643
Active, not recruiting Observational

Gingival Crevicular Fluid Biomarkers and Healing After Root Canal Treatment in Asymptomatic Apical Periodontitis

NCT07468643 · tracked via the Priya Life Science Egypt tracker
Phase
Observational
Started
2025-05-02
Last updated
2026-03-12

Condition(s) studied

Pulp and Periapical Tissue Disease

Investigational drug(s) / intervention(s)

Primary Nonsurgical Root Canal Treatment

Primary Nonsurgical Root Canal Treatment: Standardized primary nonsurgical root canal treatment will be performed in teeth diagnosed with asymptomatic apical periodontitis under rubber dam isolation. The procedure includes access cavity preparation, working length determination, chemomechanical canal preparation, irrigation using sodium hypochlorite solution, obturation of the root canal system, and placement of a coronal restoration according to standard endodontic protocols.

Study summary

This prospective observational cohort study will evaluate whether changes in gingival crevicular fluid osteoprotegerin (OPG) , RANKL/OPG ratio ,IL10,IL8and CxCL10 after primary nonsurgical root canal treatment are associated with 12-month radiographic healing in teeth with asymptomatic apical periodontitis. Participants will undergo standardized treatment and follow-up with serial GCF sampling and standardized digital periapical radiography.

Eligibility

Sex
ALL
Min age
18 Years
Max age
40 Years
Healthy volunteers
Accepted
Inclusion Criteria: Adults 18 -40 years . Presence of one permanent tooth diagnosed with asymptomatic apical periodontitis. Diagnosis confirmed by pulp necrosis or non-vital pulp and presence of a periapical radiolucency on digital periapical radiograph. Tooth indicated for primary nonsurgical root canal treatment. Tooth must be restorable and periodontally healthy. Periapical lesion detectable radiographically and suitable for follow-up evaluation. Participant able and willing to provide written informed consent. Participant willing to attend follow-up visits during the study period. Exclusion Criteria Participants will be excluded if any of the following conditions are present: Teeth previously treated with root canal treatment (retreatment cases). Teeth with acute apical abscess, swelling, or sinus tract. Teeth with combined endodontic-periodontal lesions. Periodontal pockets \>3 mm or evidence of active periodontal disease around the study tooth. Teeth with vertical root fracture, root perforation, or severe root resorption. Teeth with hopeless restorative or periodontal prognosis. Patients with systemic diseases that may affect healing (e.g., uncontrolled diabetes, immunosuppression). Pregnant or breastfeeding women. Patients currently taking systemic antibiotics, corticosteroids, or anti-inflammatory medications within the last 2 weeks. Current smokers or tobacco users. Inability to attend scheduled follow-up visits.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
ALazhar university - faculty of dental medicine for girls Cairo Egypt

More Faculty of Dental Medicine for Girls trials in Egypt

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07468643 on ClinicalTrials.gov ↗ ← All trials in Egypt