Effectiveness of Premixed Bioactive Bioceramic MTA (Neo-Putty®) in Pulpotomies Primary Teeth
Condition(s) studied
Investigational drug(s) / intervention(s)
Neo-Putty® as dressing agents in pulpotomized primary molars: Following removal of the coronal pulp with a round bur and hemostasis, the pulp stumps in the study group will be covered with Neo-Putty ® according to the manufacturer's instructions. Neo-Putty will be placed in the prepared cavity, and then covered with Vitrebond® and with a reinforced Zinc Oxide-Eugenol (IRM, Bayer-Leverkussen, Germany). In the control group, a cotton pellet moistened with full-strength FC will be placed for 5 minutes on the amputated pulp, after reaching hemostasis. The pulp stumps will be then covered by IRM
Study summary
The objective of this prospective randomized clinical trial is to assess clinically and radiographically, the effect of NeoPutty as a pulp medicament following coronal pulp amputation in human primary molars with carious pulp exposure in comparison to Formocresol (FC).
Eligibility
Primary outcome measure(s)
- Success rate of the primary molar pulpotomy — One year
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Hadassah Medical Organization | Jerusalem | Israel |
More Hadassah Medical Organization trials in Israel
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT04962607 on ClinicalTrials.gov ↗ ← All trials in Israel