Evaluation of Bacterial Reduction After Pulpectomy in Primary Molars
Ориентир для пациента и семьи
Простыми словами
Автоматическая сводка по структурированным данным реестра. Она помогает сориентироваться, но не заменяет официальный протокол или оценку врача.
- Что изучают
- В протоколе указаны: Rotary Instrumentation, Manual Instrumentation.
- Кому может быть актуально
- Состояния в реестре: Irreversible Pulpitis. Базовые параметры: 4 лет — 6 лет · Все.
- Что важно проверить
- Возраст, диагноз и пол — только базовые ориентиры. Предыдущее лечение, анализы и другие обязательные условия указаны ниже в критериях участия.
- Где проводится
- Египет
- Следующий шаг
- Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
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Официальное название
Comparative Evaluation of Bacterial Reduction Using Single Rotary File System Versus Manual Instrumentation in Pulpectomy of Primary Molars: An In Vitro and In Vivo Study
Обзор
The primary aim of the study is to compare the bacterial reduction in pulpectomy of primary molars using a single rotary file system versus conventional manual instrumentation.
Подробное описание
This study aims to compare the antibacterial effectiveness of a single rotary file system with conventional manual instrumentation during pulpectomy of primary molars. The study will evaluate bacterial reduction by microbiological culture techniques using colony-forming units per milliliter (CFU/mL) before and after chemo-mechanical preparation.
This investigation will include both in vitro and in vivo components to provide a comprehensive evaluation of bacterial reduction. In the clinical part of the study, children aged 4 to 6 years with restorable mandibular second primary molars diagnosed with irreversible pulpitis will be recruited from the outpatient clinic of the Pediatric Dentistry and Dental Public Health Department at the Faculty of Dentistry, Cairo University. Eligible teeth will undergo pulpectomy and will be randomly assigned to one of two groups:
Group 1: Pulpectomy using a single rotary file system. Group 2: Pulpectomy using conventional manual stainless-steel K-files.
Microbiological samples will be collected from the root canals before instrumentation and after completion of chemo-mechanical preparation using sterile paper points. The samples will be transferred to brain-heart infusion broth and cultured on agar plates under aerobic and anaerobic conditions. Bacterial growth will be quantified by counting colony-forming units to determine the degree of bacterial reduction produced by each instrumentation technique.
The findings of this study will contribute to evidence-based decision-making in pediatric endodontics by clarifying whether rotary instrumentation provides superior bacterial reduction compared with manual instrumentation in primary molar pulpectomy. Improved understanding of the antimicrobial effectiveness of these techniques may help clinicians select instrumentation methods that enhance treatment success, reduce chairside time, and improve patient cooperation during pediatric dental procedures.
Вмешательства
- Процедура Rotary Instrumentation
After opening the access cavity, the root canal patency will be checked for all the canals located using a size #15 (0.02%) K file, then a single rotary file (AF F One, FANTA, China) (20 taper 4) will be adjusted to the desirable working length depending on an electronic apex locator (1 mm shorter than the apex). This file will be used in the pulpectomy procedure using a brushing motion and will be irrigated with saline. - Процедура Manual Instrumentation
After opening the access cavity, manual files (K files, Mani, Inc., Japan) of sizes 15, 20, 25, and 30 will be adjusted to the desirable working length depending on an electronic apex locator (1 mm shorter than the apex). These files will be used in the pulpectomy procedure using a brushing motion and will be irrigated with saline.
Первичные конечные точки
- Intracanal Bacterial Load Reduction [Срок оценки: Immediately before instrumentation and immediately after completion of chemo-mechanical preparation during the same treatment visit.]
Вторичные конечные точки (4)
- Postoperative Pain [Срок оценки: at 6, 12, 24, 48, and 72 hours and 1 week after treatment.]
- child's behavior level. [Срок оценки: Immediately after treatment.]
- Instrumentation time [Срок оценки: during the procedure, starting from anesthesia till end of procedure]
- Clinical success [Срок оценки: At 3, 6, and 12 months]
Критерии участия
Критерии включения
- Children age 4 to 6 years
- Medically free children
- Cooperative children
- Restorable mandibular second primary molars with signs or symptoms of irreversible pulpitis
- No internal root resorption on radiograph
- No external root resorption on radiograph
- No periapical radiolucency
- No inter-radicular radiolucency
Критерии исключения
- Uncooperative children
- Children with systemic disease
- Children with physical disability
- Children with mental disability
- Refusal to participate
- Inability to attend follow-up visits
- Refusal to sign consent form
- Previously accessed teeth
- Mobile mandibular primary molars
- Pain on percussion
- Swelling on palpation or in the vestibule
Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.
Здоровые добровольцы: Нет
Дизайн исследования
- Распределение
- Рандомизированное
- Модель
- Параллельные группы
- Маскирование
- Двойное слепое
- Основная цель
- Лечение
Центры проведения
Египет · 1 центр
- Faculty of dentistry, Cairo university — Cairo
Идентификаторы
NCT: NCT07472751 · pedo-3-2026