Clinical Trials Directory

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UnknownNCT05475795

Postoperative Pain After Pulpectomy of Primary Molars Using Different Obturation Materials

Postoperative Pain After Pulpectomy of Primary Molars Using Different Obturation Materials: A Parallel Randomized Clinical Trial

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
150 (estimated)
Sponsor
Minia University · Academic / Other
Sex
All
Age
5 Years – 7 Years
Healthy volunteers
Accepted

Summary

Testing postopertive pain after pulpectomy of primary molars with Metapex and Endoflas using modified Wong-Baker scale of pain.

Detailed description

The current equivalent parallel randomized controlled trial will be conducted to evaluate intensity and duration of post-operative pain after pulpectomy of asymptomatic necrotic primary molars, using Metapex and Endoflas obturation materials

Conditions

Interventions

TypeNameDescription
OTHERMetapexobturation of root canals of primary molars with Metapex
OTHEREndoflasobturation of root canals of primary molars with Endoflas

Timeline

Start date
2022-06-09
Primary completion
2022-12-15
Completion
2023-01-16
First posted
2022-07-27
Last updated
2022-08-02

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT05475795. Inclusion in this directory is not an endorsement.