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Assessment of Postoperative Pain of Two Bioceramic Root Canal Sealers With Obturation Techniques

NCT06075550 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 60

Last updated 2023-10-10

No results posted yet for this study

Summary

60 patients were divided into 2 groups, 30 patient in each group

Group I: Obturation with TotalFill BC Sealer using the single cone technique

Group II: Obturation with TotalFill BC Sealer HiFlow using the warm vertical compaction technique.

Every participant will be given a Visual Analog Scale (VAS) to record the intensity of postoperative pain at 6 hr, 24 hr, 48 hr, 72 hr, and 1week after treatment. The patients will return their Visual Analog Scale (VAS) after 1 week and the recorded pain data will be collected and statistically analyzed regarding each group.

Conditions

  • Effect of Material and Technique

Interventions

OTHER

single cone technique using TotalFill BC Sealer

Gutta percha cone size X5 (Dentsply, Maillefer) TotalFill BC Sealer (FKG Dentaire SA, La Chaux-de-Fonds, Switzerland)

OTHER

warm vertical compaction technique using TotalFill BC Sealer HiFlow

TotalFill BC Sealer HiFlow (FKG Dentaire SA, La Chaux-de-Fonds, Switzerland)

Sponsors & Collaborators

  • Minia University

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
20 Years
Max Age
50 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2021-06-02
Primary Completion
2021-09-16
Completion
2022-03-20

Countries

  • Egypt

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06075550 on ClinicalTrials.gov