Evaluation of Post Operative Pain After Using Two Different Types of Sealers

Post Operative Pain Clinical Trial

Official title:

Evaluation of Post Operative Pain After Using Two Different Types of Sealers (a Randomized Clinical Trial )

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05729893
• Other study ID #: BritishUE sara
• Status: Recruiting
• Phase: N/A
• Start date: February 1, 2023
• Est. completion date: September 1, 2023

Study information

• Verified date: February 2023
• Source: British University In Egypt
• Contact: sara tarek mohamed, bachelor
• Phone: 01007434392
• Email: sara.alsayed[@]bue.edu.eg
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

conventional endodontic treatment is done using two different types of sealers in the obturation to evaluate the post operative pain between the two sealers

Description:

STUDY WILL BE PERFORMED ON PATIENTS DIAGNOSED WITH SYMPTOMATIC IRREVERSABE PULPITIS.

TREATMENT PROTOCOL FOR ALL PATIENTS IS CONVENTIONAL ROOT CANAL TREATMENT

ACCESS CAVITY AND CLEANING AND SHAPING PROCEDURES WILL BE EXECUTED FOR ALL PATIENTS WITH THE SAME PROTOCOL

SELECTED PATIENTS WILL THEN BE DIVIDED INTO TWO GROUPS,

GROUP1: ALL CANALS WILL BE OBTURATED USING RESIN STANDARD SEALERS.

GROUP2: ALL CANALS WILL BE OBTURATED USING HIGH FLOW BIOCERAMIC SEALERS THAT ACCEPT WARM VERTICAL COMPACTION

POST OPERATIVE PAIN IN THE TWO GROUPS WILL BE EVALUATED USING THE VISUAL ANALOUG SCALE AND COMPARED AT DIFFERENT TIME PERIODS (12H, 24H, 48H, 72H)

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 40
• Est. completion date: September 1, 2023
• Est. primary completion date: June 1, 2023
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 50 Years

Eligibility

Inclusion Criteria:

• • Patients age ranges from 18-50 years old.

• Patients with teeth diagnosed with symptomatic irreversible pulpitis.

• Normal periapical condition confirmed by normal periapical radiograph or that with minimal widening of the PDL space

• The teeth are restorable

• Teeth are periodontally free.

Exclusion Criteria:

• • Teeth with immature roots

• Non restorable teeth

• Medically compromised patients with systemic complication that would alter the treatment.

• Necrotic teeth

• Teeth with apical periodontitis or periapical lesions

• Teeth that need multiple visits treatment

Related Conditions & MeSH terms

• Pain, Postoperative
• Post Operative Pain

Intervention

Other:
• root canal sealers
different sealer used in obturating root canals (resin and bio ceramic)

Locations

Country	Name	City	State
Egypt	British university in egypt	Cairo

Sponsors (1)

Lead Sponsor	Collaborator
British University In Egypt

Country where clinical trial is conducted

Egypt, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Pain level comparison after root canal obturation with two different endodontic sealers: VAS (Visual Analogue Scale) at 12 hours	Based on the VAS (Visual Analogue Scale), the pain levels of the patients were assessed. The scale consisted of a 100-mm-long line divided into 10 equal intervals from 0 (no pain) to 100 (very severe pain). Every patient was asked to mark his or her perceived postoperative pain level on the line.	12 hours
Primary	Pain level comparison after root canal obturation with two different endodontic sealers: VAS (Visual Analogue Scale) at 24 hours	Based on the VAS (Visual Analogue Scale), the pain levels of the patients were assessed. The scale consisted of a 100-mm-long line divided into 10 equal intervals from 0 (no pain) to 100 (very severe pain). Every patient was asked to mark his or her perceived postoperative pain level on the line.	24 hours
Primary	Pain level comparison after root canal obturation with two different endodontic sealers: VAS (Visual Analogue Scale) at 48 hours	Based on the VAS (Visual Analogue Scale), the pain levels of the patients were assessed. The scale consisted of a 100-mm-long line divided into 10 equal intervals from 0 (no pain) to 100 (very severe pain). Every patient was asked to mark his or her perceived postoperative pain level on the line.	48 hours
Primary	Pain level comparison after root canal obturation with two different endodontic sealers: VAS (Visual Analogue Scale) at 72 hours	Based on the VAS (Visual Analogue Scale), the pain levels of the patients were assessed. The scale consisted of a 100-mm-long line divided into 10 equal intervals from 0 (no pain) to 100 (very severe pain). Every patient was asked to mark his or her perceived postoperative pain level on the line.	72 hours