About this trial
This randomized clinical trial aims to compare the clinical and radiographic success of calcium hydroxide-iodoform paste and modified triple antibiotic paste when used for the treatment of necrotic primary molars in children using the lesion sterilization and tissue repair (LSTR) technique. The study will include children aged 4-7 years with restorable necrotic mandibular second primary molars. Participants will be randomly assigned to receive LSTR treatment with either calcium hydroxide-iodoform paste or modified triple antibiotic paste. Clinical and radiographic findings will be assessed during follow-up over 12 months to determine the success of each treatment. The study hypothesis is that there will be a difference in the clinical and radiographic success between the two treatment materials when used with the LSTR technique
Eligibility criteria
Qualifiers
Pediatric patients aged 4-7 years
Positive parental informed consent
Restorable necrotic mandibular second primary molars with peri-radicular/furcal involvement and/or pathologic root resorption (external or internal one-third to two-thirds of the root)
Presence of chronic apical abscess or sinus tract or furcation radiolucency
Disqualifiers
Medically compromised patient
Children with a known allergy to any of the components being utilized
Molars near exfoliation
Molars with severely resorbed roots more than two thirds, indicated for extraction
Trial design
Treatments tested in this trial
- Calcium Hydroxide, Iodoform, paste
- modified triple antibiotic paste