ClinicalTrials.Veeva

Menu

Analyzing the Impact of Occlusal Reduction on the Pain Following Root Canal Therapy in Molar Teeth With and Without Pain in Turkish Patients.

S

Sakarya University

Status

Completed

Conditions

Irriversible Pulpitis

Treatments

Other: occlusal reduction

Study type

Interventional

Funder types

Other

Identifiers

NCT06953856
E-71522473-050.01.04-39802-329

Details and patient eligibility

About

Introduction: This study aimed to compare the intensity of postoperative pain after single-visit root canal treatment of symptomatic or asymptomatic teeth following occlusal reduction.

Methods: A total of 140 symptomatic or asymptomatic patients in need of root canal therapy were registered in this prospective, single-center, single-blind, randomized clinical trial.

For all patients, root canal treatment was carried out in a single visit, and the teeth were restored using composite resin. The teeth were randomly allocated into two equal groups according to whether occlusal reduction was done or not. The patients' pain were assessed using a 0-3 verbal rate scale 1, 3, and 7 days following root canal treatment. The pain incidence and intensity were compared using the chi-square and Fisher's exact tests.

Full description

Root canal treatments is usually associated with post-operative pain and this is a bothersome situation for both patient and practitioner. Due to this reason number of researches focus on the factors that may relief patients pain. Occlusal reduction is one of the factors that means the chewing surface of the teeth are cut off and no longer in contact.Despite the large number of studies on this subject, no consensus has been reached. Decoupling group standardization and arriving at a more consistent conclusion were the goals of this research. The aim of this research is to evaluate the impact of occlusal reduction on postoperative pain in both symptomatic and asymptomatic molar teeth.

Enrollment

140 patients

Sex

All

Ages

18 to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Healty patients
  • Maxillary and mandibulary first and second molars
  • Irriversible pulpitis cases with or without prior discomfort

Exclusion criteria

  • Patients under 18 years old,
  • Patients older 65 years old,
  • Teeth with previously undergone root canal treatment,
  • Complicating systemic diseases,
  • Allergies o local anesthetic agents,
  • Presence of acute apical apsesses,
  • History of trauma,
  • Analgesic, antibiotic or antiinflamatory intake 7 days before treatment,
  • Periodontal pockets deeper than 4 mm,
  • Multiple teeth that require endodontic treatment,
  • Pregnancy,
  • Teeth that can not be restored,
  • Patients who needed emergency treatment,
  • Grade 2 or 3 mobility,
  • Patients with bruxism

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Factorial Assignment

Masking

Single Blind

140 participants in 2 patient groups

Occlusal reduction,
Other group
Description:
one of the group received occlusal reduction after root canal treatment while other did not.
Treatment:
Other: occlusal reduction
no occlusal reduction
No Intervention group
Description:
this group did not receive any occlusal reduction after root canal treatment.

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems