Postoperative Pain After Pulpectomy of Primary Molars
Launched by MINIA UNIVERSITY · May 16, 2024
Trial Information
Current as of February 19, 2025
Recruiting
Keywords
ClinConnect Summary
This clinical trial is focused on understanding the level of pain children experience after a specific dental procedure called pulpectomy, which is a treatment for decayed primary molars (the baby teeth). The researchers will use a simple pain scale called the modified Wong-Baker scale to measure how much pain the children feel after their treatment. They are currently looking for children aged 5 to 7 who have deep cavities in their primary molars but are otherwise healthy and show no signs of current pain.
To be eligible for this study, children should not have any serious dental issues, like a toothache that happens without being triggered or severe damage to the tooth that makes it hard to fix. Participating children will receive care for their dental needs, and their pain levels will be monitored after the procedure to help improve future treatments. This trial aims to gather important information that can help dentists better manage pain in young patients undergoing similar procedures.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- * The current study will include children who meet the following clinical and radiographic criteria:
- 3.1a.Clinical:
- • 1. 5-7-year old children categorized as class I or II according to American Society of Anaesthesiologists (ASA) scale.
- • 2. Children rated as no.3 or 4 in Frankel behavior rating scale (FBRS).
- • 3. Presence of at least one primary molar with deep carious lesion.
- • 4. Asymptomatic necrotic molars confirmed by the absence of bleeding on opening of the pulp chamber.
- 3.1b. Radiographic:
- • 1. Extensive caries approaching to the pulp.
- • 2. Presence of at least two-thirds of root length.
- Exclusion Criteria:
- * A child's tooth with any of the following criteria:
- 3.2a. Clinical findings:
- • 1. History of spontaneous unprovoked toothache.
- • 2. Extensive crown destruction that preclude coronal restoration.
- • 3. Presence of adjacent or opposing tooth with deep carious lesion "in the same side".
- • 4. History of administering analgesics 12 hours before tooth obturation.
- 3.2b. Radiographic findings:
- • 1. Presence of a large furcation or periapical radiolucency approximating the succedaneous tooth.
- • 2. Presence of pathological internal/external root resorption.
- • 3. Absence of underlying permanent successor.
Trial Officials
osama s gad elhak, phD
Study Director
Pediatric Dentistry Department, Faculty of Dentistry, Minia University
About Minia University
Minia University is a prestigious educational institution located in Egypt, dedicated to advancing medical research and clinical trials. With a commitment to fostering innovation and improving healthcare outcomes, the university collaborates with a diverse range of stakeholders, including healthcare professionals and researchers. Minia University aims to enhance clinical practices through rigorous research methodologies and ethical standards, contributing to the body of knowledge in the medical field while addressing local and global health challenges. The university's clinical trial initiatives are designed to evaluate new treatments and interventions, ensuring a positive impact on patient care and community health.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Minya, , Egypt
People applied
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
Discussion 0