Different intracanal medicines for retreatment of lower first molars
Official title: Biological, Radiographic and Clinical Evaluation of Various Inter-Visit Root Canal Dressings in Retreatment Cases: A Randomized Controlled Clinical Trial
Run by Ain Shams University · NCT07641933 · Data updated 2026-11-12
This study tests three intracanal medications to see which best reduces inflammation, heals lesions, and relieves pain in retreatment of a lower first molar with a periapical lesion.
Quick facts
| Phase | Phase 1 |
|---|---|
| Study type | Interventional |
| Ages | 21 Years to 45 Years |
| Sex | All |
| Enrollment | 60 (estimated) |
| Sponsor | Ain Shams University Academic / other |
| Locations | 1 site (Cairo) |
| Status | Recruiting |
| Started | June 1, 2026 |
| Main results expected | June 2027 |
| Study ends | August 2027 |
| Registry record updated | June 12, 2026 |
| Trial ID | NCT07641933 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults 21–45 years, ASA I, with restorable lower first molars and small to medium periapical lesions undergoing retreatment.
✕Probably not a fit
Patients with allergies to study materials, non-restorable teeth, mobility or deep periodontal pockets, or resorption may not benefit.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This is a randomized, single-center phase 1 interventional study comparing three intracanal medications used during retreatment of failed lower first molars with periapical lesions. Patients are allocated equally to calcium hydroxide slurry with sodium hypochlorite, calcium silicate, or calcium hydroxide as the intracanal medicament. Outcomes include inflammatory biomarker IL-1β from periapical fluids, radiographic lesion size by CBCT, and patient-reported pain scores over time. Assessments occur after the second visit (two weeks) and up to 12 months post-treatment to evaluate inflammation reduction, lesion healing, and pain trajectories.
Why it matters
Potential benefit: If successful, the preferred medicament could better control inflammation and promote faster healing after retreatment.
How similar studies have gone: Prior work suggests intracanal medications can influence inflammation and healing, but this exact multi-arm comparison in retreatment is novel.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: 1. Age: 21-45 years. 2. Medically free patients. (ASA Class 1) 3. Gender: males and females 4. Patients who are cooperative at operation and in attendance at scheduled follow-up visits. 5. Restorable root canal treated permanent lower first molars with periapical lesions. 6. Small (\<5 mm) or medium periapical lesion size (5-10 mm) Exclusion Criteria: 1. Patients with a history of allergic reactions to any of the study materials. 2. Teeth that become non-restorable after complete caries excavation. 3. Teeth that have mobility or deep periodontal pockets. 4. Teeth with internal or external resorption.
Where it's running
-
Ain Shams University
Cairo, Egypt Recruiting
Study contacts
- Study coordinator: Merna Mamdouh Botros Billatos, Msc
- Email: mernabotros@dent.asu.edu.eg
- Phone: 00201201579537
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.