Occlusal Reduction Effect on Postendodontic Pain

NCT04186897 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 308

Last updated 2019-12-06

No results posted yet for this study

Summary

The aim of this study, thus, was to assess the effect of occlusal reduction on postendodontic pain after the first (post-instrumentation) and the second (post-obturation) visit in mandibular posterior teeth with symptomatic irreversible pulpitis and sensitivity to percussion treated in two visits.

Conditions

  • Symptomatic Irreversible Pulpitis

Interventions

PROCEDURE

Occlusal reduction

Occlusal contacts on the functional and non-functional cusps were reduced.

PROCEDURE

Sham occlusal reduction

The occlusal surface left intact. No actual occlusal reduction.

Sponsors & Collaborators

  • Cairo University

    lead OTHER

Principal Investigators

  • Randa El Boghdadi, PhD · Cairo University

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2014-09-30
Primary Completion
2016-12-31
Completion
2016-12-31

More Related Trials

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 NCT04186897 on ClinicalTrials.gov