NCT05860712 Evaluation of Antimicrobial, Post Operative Pain of Cinnamon Extract Versus Sodium Hypochlorite Irrigant Following Pulpectomy of Primary Teeth
| NCT ID | NCT05860712 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Cairo University |
| Condition | Irreversible Pulpitis |
| Study Type | INTERVENTIONAL |
| Enrollment | 26 participants |
| Start Date | 2024-01-20 |
| Primary Completion | 2024-09-20 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.
This trial targets 26 participants in total. It began in 2024-01-20 with a primary completion date of 2024-09-20.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
The aim of the study is to evaluate effectiveness of cinnamon extract versus sodium hypochlorite as root canal irrigant for in pulpectomy of primary teeth in reduction of bacterial count .
Eligibility Criteria
Inclusion Criteria: * Children: 1. Aged 4 to 8, in good general health, and medically free. 2. Cooperative patients who will comply to dental treatment . 3. Parents provided with written informed consent. 4. No previous history of antibiotics administration or last dose was taken from at least 2 weeks. * Teeth: 1. Carious primary molars with irreversible pulpitis. 2. Presence of localized swelling ,sinus and pain on percussion which indicate non vital pulp . 3. Presence of periapical and furcation radiolucency . 4. In periapical radiograph teeth have no more than 1/3 of root resorption. Exclusion Criteria: * Children: 1. Children with medical, physical, or mental conditions. 2. Severly Uncooperative children . * Teeth: 1. Primary molars with any congenital anomalies. 2. Teeth with un-restorable crowns . 3. Root resorbtion more than half of the root. \-
Frequently Asked Questions
Who can join the NCT05860712 clinical trial?
This trial is open to participants of all sexes, aged 4 Years or older, up to 8 Years, studying Irreversible Pulpitis. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT05860712 currently recruiting?
Yes, NCT05860712 is actively recruiting participants. Visit ClinicalTrials.gov or contact Cairo University to inquire about joining.
Where is the NCT05860712 trial being conducted?
This trial is being conducted at Cairo, Egypt.
Who is sponsoring the NCT05860712 clinical trial?
NCT05860712 is sponsored by Cairo University. The trial plans to enroll 26 participants.