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Evaluation of Different Materials in Pulpotomy of Primary Molars

NCT05981352 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 36

Last updated 2023-08-24

No results posted yet for this study

Summary

The aim of the current study is to evaluate and compare clinical and radiographic success and antibacterial effect of Hyaluronic Acid and Amniotic membrane pulpotomy in primary molars in comparison with MTA pulpotomy (Randomized Clinical Trial and In Vitro Study).

Conditions

  • Pulp Disease, Dental

Interventions

PROCEDURE

mineral trioxide aggregate pulpotomy

* After achieving hemostats, Mineral trioxide aggregate powder will be mixed with saline. * Then Mineral trioxide aggregate will be placed directly on the pulp stumps.

PROCEDURE

Dehydrated amniotic membrane pulpotomy

* After achieving haemostasis, a double layer of sterile processed human allograft tis¬sue (dehydrated dual-layer dental amni¬on patch) will be trimed and soaked in saline for a minute. * Dehydrated amniotic membrane will be Placed directly on the pup stumps using sterile tweezers and adjust¬ed to the entire floor of the pulp chamber.

PROCEDURE

Hyaluronic acid pulpotomy

* After achieving haemostasis, pulp stumps will be covered with a mixture of Hyaluronic acid gel and zinc oxide powder with consistency (1:1 ratio by volume) . * The cavities of all pulpotomy molars will be sealed with a layer of reinforced zinc oxide and eugenol .

Sponsors & Collaborators

  • Ain Shams University

    lead OTHER

Principal Investigators

  • eman Ib Abdel Maksoud, doctor · Ain Shams University

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
4 Years
Max Age
8 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-10-31
Primary Completion
2024-10-01
Completion
2024-10-01

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05981352 on ClinicalTrials.gov