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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).
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Study Group |
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| control group |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Neo-Putty® as dressing agents in pulpotomized primary molars | Other | 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 |
| Measure | Description | Time Frame |
|---|---|---|
| Success rate of the primary molar pulpotomy | One year |
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Inclusion Criteria:
Exclusion Criteria:
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Healthy children attending the Pediatric Dentistry Clinic of the Hebrew University-Hadassah School of Dental Medicine in Jerusalem
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Hadassah Medical Organization | Jerusalem | 91120 | Israel |
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