About this trial
This randomized clinical study evaluates the antibacterial effectiveness and postoperative pain following root canal irrigation using the Triton irrigation protocol in necrotic mandibular molars. Thirty-six patients requiring root canal treatment will be included. The study aims to compare bacterial reduction and postoperative pain outcomes after treatment. Results may help improve irrigation protocols and patient comfort during endodontic therapy.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
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
Disqualifiers
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.
Trial design
Parallel
Treatments tested in this trial
triton irrigation protocol
Procedure/SurgeryRoot canal irrigation performed using Triton solution according to a standardized endodontic irrigation protocol during root canal treatment.
conventional irrigation group
Procedure/SurgeryParticipants receive conventional root canal irrigation using standard irrigation solutions during chemo-mechanical preparation according to the routine clinical protocol.
Treatment groups
Trial outcomes
Primary outcomes
antibacterial effect
Reduction in bacterial count will be evaluated by microbiological sampling before and after irrigation.
Secondary outcomes
postoperative pain intensity
Postoperative pain will be assessed using a Visual Analog Scale (VAS) following root canal treatment with different irrigation protocols.
Sponsors and contacts
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sara hosny mostafa
Lead sponsor
Future University in Egypt
Sponsor institution
This trial is not recruiting at the moment. You can still explore other options: