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NCT05057325 Clinical Trial

Post Operative Pain Assessment After Pulpectomy of Primary Molars With Two Different Rotary Systems

Pulp Necroses Clinical Trial

Official title:
Post Operative Pain After Pulpectomy of Primary Molars With One Shap Rotation File Versus Wave One Reciprocating File

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT05057325
Other study ID # 605
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 10, 2021
Est. completion date June 10, 2021

Study information
Verified date August 2021
Source Minia University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Evaluation of post operative pain after pulpectomy procedures for primary molars with irreversible pulp damage and without periapical radulicency using two different systems (One shape file ( ratation movemont) and wave one gold file ( reciprocation movement)

Recruitment information / eligibility
Status Completed
Enrollment 164
Est. completion date June 10, 2021
Est. primary completion date May 10, 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 4 Years to 8 Years
Eligibility Inclusion Criteria: - Age of more than 4 years - Healthy children - Primary molars with irreversible pulp damage Exclusion Criteria: - Presence of periapical radiolucency realtes to primary molar - Uncooperative child

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• Pulpectomy using single file system ( One Shape file)
Rotary file instrument for pulpectomy of primary molars ( One shape file)
• Pulpectomy using single file system ( WaveOne Gold file)
Rotary file instrument for pulpectomy of primary molars ( WaveOne Gold file)

Locations
Country Name City State
Egypt Minia University Minya

Sponsors (1)
Lead Sponsor Collaborator
Minia University

Country where clinical trial is conducted

Egypt, 

Outcome
Type Measure Description Time frame Safety issue
Primary Post operative pain Assessment of pain using 4 piont intensity scale
1 means no pain, 2 means slight pain, 3 means moderate pain and for means sever pain at 6,12, 48,72 hours and 1 week		 1 week
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