Clinical Trials Directory

Trials / Completed

CompletedNCT04186897

Occlusal Reduction Effect on Postendodontic Pain

Postendodontic Pain Following Occlusal Reduction in Mandibular Posterior Teeth: a Single-centre Randomized Controlled Trial

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
308 (actual)
Sponsor
Cairo University · Academic / Other
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Not accepted

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.

Detailed description

The purpose of this randomized clinical trial was to evaluate the effect of occlusal reduction on post-instrumentation and post-obturation pain in mandibular posterior teeth with symptomatic irreversible pulpitis and sensitivity to percussion treated in two visits. Three hundred and eight patients were included in this study. Inclusion criteria were posterior mandibular teeth having symptomatic irreversible pulpitis with sensitivity to percussion. Patients were randomized into two equal groups. In the intervention group, occlusal reduction was done, while, in the control group, the occlusal surfaces were left intact. Conventional endodontic treatment was performed in two visits using a rotary nickel-titanium system followed by the lateral-condensation obturation technique. Post-instrumentation pain was assessed after 6, 12, 24 and 48 hours following the first visit, and post-obturation pain after 6 and 12 hours following the second visit. Each patient received a pain diary to record their pain levels and rescue medication intake.

Conditions

Interventions

TypeNameDescription
PROCEDUREOcclusal reductionOcclusal contacts on the functional and non-functional cusps were reduced.
PROCEDURESham occlusal reductionThe occlusal surface left intact. No actual occlusal reduction.

Timeline

Start date
2014-09-01
Primary completion
2016-12-01
Completion
2016-12-01
First posted
2019-12-05
Last updated
2019-12-06

Source: ClinicalTrials.gov record NCT04186897. Inclusion in this directory is not an endorsement.