Comparing outcomes of partial pulpotomy in children's molars using different materials and methods
Clinical and Radiographic Outcomes of Partial Pulpotomy Procedure in Primary Molars Utilizing Different Capping Materials and Different Restorative Methods: A Randomized Clinical Trial
This study is testing different materials and methods for a dental procedure in kids' molars to see which one helps keep their teeth healthy and working well.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 84 (estimated) |
| Ages | 4 Years to 7 Years |
| Sex | Male |
| Sponsor | British University In Egypt Academic / other |
| Locations | 1 site (Cairo) |
| Trial ID | NCT06227390 on ClinicalTrials.gov |
What this trial studies
This clinical trial aims to evaluate the clinical and radiographic outcomes of partial pulpotomy procedures in vital primary molars. It will compare the effectiveness of different capping materials, including TheraCal PT®, Biodentin®, and NeoPUTTY® MTA, followed by either glass ionomer restoration alone or in combination with a stainless-steel crown. The study focuses on maintaining the vitality and function of primary teeth, which are crucial for children's dental health and development. By utilizing less invasive techniques, the trial seeks to improve treatment outcomes for children with deep carious lesions.
Who should consider this trial
Good fit: Ideal candidates for this study are healthy children aged 4-7 years with asymptomatic primary molars that have deep caries requiring vital pulp therapy.
Not a fit: Patients with a history of pain, swelling, or other complications related to their dental condition may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could enhance the preservation of primary molars in children, leading to better dental health and function.
How similar studies have performed: Other studies have shown promising results with similar approaches in vital pulp therapy, indicating potential for success in this trial.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: 1. Healthy patients aged 4-7-years old. 2. Cooperative patients (Frankle scale + and ++) 3. Asymptomatic primary molar with deep caries requiring vital pulp therapy Exclusion Criteria: * presence of any of the following: 1. History of spontaneous lingering pain, swelling, or sinus tract. 2. Pathological mobility. 3. pain on percussion. 4. Furcation or periapical radiolucency. 5. pathological root resorption
Where this trial is running
Cairo
- the British University in Egypt — Cairo, Egypt (Recruiting)
Study contacts
- Study coordinator: ali Mohamed elsharkawy, master candidate
- Email: ali.elsharkawy@bue.edu.eg
- Phone: 01003088299
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.