Postoperative Pain After Pulpectomy of Primary Molars

Postoperative Pain Clinical Trial

Official title:

Postoperative Pain After Pulpectomy of Primary Molars Using Two Different Root Canal Obturation Techniques: A Randomized Clinical Trial

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT06424353
• Other study ID #: 87-577
• Status: Recruiting
• Phase: N/A
• Start date: January 20, 2024
• Est. completion date: June 2024

Study information

• Verified date: May 2024
• Source: Minia University
• Contact: shimaa m abd elhafeez, postgraduate
• Phone: +0201068976757
• Email: drshimaaalhhafeez93[@]gmail.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

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

Description:

Testing postopertive pain after pulpectomy of primary molars with endoflas using lentilospiral files and pressure seringe by using modified Wong-Baker scale of pain.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 100
• Est. completion date: June 2024
• Est. primary completion date: May 2024
• Accepts healthy volunteers: No
• Gender: All
• Age group: 5 Years to 7 Years

Eligibility

Inclusion Criteria:

• The current study will include children who meet the following clinical and radiographic criteria:

3.1a.Clinical:

1. 5-7-year old children categorized as class I or II according to American Society of Anaesthesiologists (ASA) scale.

2. Children rated as no.3 or 4 in Frankel behavior rating scale (FBRS).

3. Presence of at least one primary molar with deep carious lesion.

4. Asymptomatic necrotic molars confirmed by the absence of bleeding on opening of the pulp chamber.

3.1b. Radiographic:

1. Extensive caries approaching to the pulp.

2. Presence of at least two-thirds of root length.

Exclusion Criteria:

• A child's tooth with any of the following criteria:

3.2a. Clinical findings:

1. History of spontaneous unprovoked toothache.

2. Extensive crown destruction that preclude coronal restoration.

3. Presence of adjacent or opposing tooth with deep carious lesion "in the same side".

4. History of administering analgesics 12 hours before tooth obturation.

3.2b. Radiographic findings:

1. Presence of a large furcation or periapical radiolucency approximating the succedaneous tooth.

2. Presence of pathological internal/external root resorption.

3. Absence of underlying permanent successor.

Related Conditions & MeSH terms

• Pain, Postoperative
• Postoperative Pain

Intervention

Procedure:
• Endoflas pulpectomy
obturation of root canals of primary molars with Endoflas using pressure seringe and lentilospiral files

Locations

Country	Name	City	State
Egypt	Shimaa Mohamed Abd Elhafeez	Minya

Sponsors (1)

Lead Sponsor	Collaborator
Minia University

Country where clinical trial is conducted

Egypt, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	postoperative pain	Measuring post operative pain after pulpectomy with two different obturation techniques using (Modified Wong-backer scale of pain )which have four scales from( 0 to 3) which 0 is the better outcome( no pain) and 3 is the worst (severe pain)	after one day and after one week