Clinical Efficacy of Novel Jasminum-based Calcium Hydroxide Medicament
Pakistan60 participantsStarted 2024-04-24
Plain-language summary
A triple-blind, parallel group, randomized trial with an allocation ratio of 1:1. Participants randomly allocated into two groups A and B. In group A, nano-reinforced calcium hydroxide medicament was utilized while in group B, calcium hydroxide medicament without nanoparticles was used. Post-operative pain was assessed after 4 hours, 24 hours, 48 hours, 72 hours, 96 hours.
Who can participate
Age range18 Years – 50 Years
SexALL
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Participants with good general health status
* Necrotic pulp with Symptomatic Apical Periodontitis
* Single rooted teeth
Exclusion Criteria:
* Non-restorable teeth
* Teeth associated with acute or chronic apical abscess
* Teeth with chronic periodontitis
* Teeth with anatomical complexities or complications like open apex, calcified canal, severe root dilaceration, root resorptive defects
* Participants who received antibiotic treatment during the last 3 months
* Pregnant females
* Participants on pre-treatment analgesics