The effect of two different irrigation needles on post-operative pain after pulpectomy in primary molar teeth: a randomized clinical study

Not Applicable

Completed

• Conditions: maxiÅŸÅŸary primary molar teeth requiring pulpectomy; needle, pedodontics, postoperative pain

• Registration Number: TCTR20190719002
• Lead Sponsor: no

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Completion: 2019-06-10
• Study Start: 2019-07-19
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 100

Inclusion Criteria

-Upper primary molar teeth requiring pulpectomy
-Patients with no history of taking analgesics and antibiotic 12 hours before the pulpectomy
-Cooperative patients in ages ranging from 6 to 9 years
-Absence of internal or external pathologic root resorption
-Presence of adequate coronal tooth structure
-Two-thirds of each root remaining
-Parent or guardian agree for participant to take part in the study

Exclusion Criteria

-Excessive mobility (greater than grade 1 mobility)
-Children with underlying systemic disease
-Children with special health care needs

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Pain 1 week VAS

Secondary Outcome Measures

Name	Time	Method
Postoperative percussion pain 1 week VAS