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Active, not recruiting Observational

Effectiveness of Premixed Bioactive Bioceramic MTA (Neo-Putty®) in Pulpotomies Primary Teeth

NCT04962607 · tracked via the Priya Life Science Israel tracker
Phase
Observational
Started
2021-09-01
Last updated
2025-06-13

Condition(s) studied

Pulpotomies on Primary Molars

Investigational drug(s) / intervention(s)

Neo-Putty® as dressing agents in pulpotomized primary molars

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

Sex
ALL
Min age
2 Years
Max age
10 Years
Healthy volunteers
Accepted
Inclusion Criteria: * primary teeth which requires pulpotomy. Exclusion Criteria: * not healthy patients, * teeth which requires pulpectomy.

Primary outcome measure(s)

  • Success rate of the primary molar pulpotomy — One year

Trial sites (1)

FacilityCityRegionStatus
Hadassah Medical Organization Jerusalem Israel
Official registry record

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