Antibacterial Efficacy of Bioceramic and Calcium Hydroxide Intracanal Medicaments (NCT07671326) | Clinical Trial Compass
RecruitingNot Applicable
Antibacterial Efficacy of Bioceramic and Calcium Hydroxide Intracanal Medicaments
Turkey (Türkiye)24 participantsStarted 2025-10-15
Plain-language summary
This study evaluates the antibacterial effectiveness of two different intracanal medicaments, Bio-C Temp and UltraCal XS , in mandibular molar teeth with chronic apical periodontitis. Intracanal bacterial load is assessed before and after root canal preparation, after intracanal medicament removal, and after final irrigation using droplet digital PCR.
Who can participate
Age range
18 Years – 65 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Patients aged between 18 and 65 years
* Being systemically healthy (ASA I or ASA II)
* Mandibular molar teeth with a radiographically detectable radiolucent lesion in the periapical region
* Willingness of the volunteer or their legal representative to participate in the study by signing the Informed Consent Form
Exclusion Criteria:
* Patients who have received antibiotics or corticosteroids within the last 3 months
* Patients with systemic diseases
* Teeth that cannot be properly isolated with a rubber dam
* Teeth with periodontal pockets \>4 mm and teeth with crown/root fractures
* Individuals who are undergoing or planning to start orthodontic treatment during the study period
* Pregnant or breastfeeding individuals
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
Reduction in Intracanal Bacterial Load
Timeframe: From baseline microbiological sampling during the first appointment to post-medication and final irrigation sampling at the second appointment after 14 days.