Clinical Trial

Clinical and Radiographic Outcomes of Rotary Instrumentation in Primary Molars

Not Yet Recruiting
View on ClinicalTrials.gov →
Summary
This study will evaluate the clinical and radiographic outcomes of rotary versus manual pulpectomy in children with irreversible pulpitis.A single-visit pulpectomy will be performed for all patients. Participants will be allocated to rotary instrumentation using Fanta AF Baby files or manual step-back instrumentation with K-files. Canals will be irrigated with 17% EDTA and 1% sodium hypochlorite, obturated with Metapex, and restored with glass ionomer cement and stainless-steel crowns. Primary outcomes will assess clinical success at 3, 6, 9, and 12 months, while secondary outcomes will evaluate postoperative pain and radiographic success at 6 and 12 months.
Trial Details
NCT Number NCT07319741
Lead Sponsor Anfal mohamed elmotaz almogtaba
Collaborators: Cairo University
Conditions Pulpectomy, Irreversible Pulpitis
Enrollment 44 participants
Start Date 2026-02
Primary Completion 2027-02 (estimated)
Study Completion 2027-02 (estimated)
Updated on ClinicalTrials.gov 2026-01-06