Clinical and Radiographic Outcomes of Rotary Instrumentation in Primary Molars
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age5-7
SponsorAnfal mohamed elmotaz almogtaba
About this trial
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.
Eligibility criteria
Qualifiers
Children aged 5-7 years with irreversible pulpitis of primary molars.
History of spontaneous pain with a deep carious lesion.
Parents who approve to write informed consent.
Disqualifiers
Medically compromised children.
Children with a history of allergic reaction to the materials used in the study.
Children with non-restorable teeth.
Teeth with resorbed roots (more than two-thirds of root length).
Trial design
Treatments tested in this trial
- Rotary Instrumentation
- Manual Instrumentation
Treatment groups
44 Participants
are divided into 2 treatment groupsSponsors and collaborators
Anfal mohamed elmotaz almogtaba
Lead sponsor
Cairo University
Sponsor institution
Cairo University
Collaborator
Source ClinicalTrials.gov