Skip to main content
Clinical Trials/NCT04358861
NCT04358861CompletedNot Applicable

Healing Outcome of Nonsurgical Root Canal Treatment in Maxillary Molars With Dental Operating Microscope : A Randomized Controlled Trial

Postgraduate Institute of Dental Sciences Rohtak1 site in 1 country67 target enrollmentStarted: January 1, 2018Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
67
Locations
1
Primary Endpoint
Clinical and radiographic success

Study Overview

Brief Summary

The aim of study was to evaluate the effect of dental operating microscope use on the healing outcome of non surgical endodontic treatment of maxillary molars.

Detailed Description

Prior to treatment a thorough clinical and radiological examination was carried out. A thorough history was taken from each patient and written informed consent was taken after explaining the procedure, risks and benefits. Mature maxillary first permanent molar with diagnosis of periapical periodontitis (as confirmed clinically & by periapical radiograph) was chosen for the study. Fifty participants were randomly assigned to either the dental operating microscope group or to control group (without using dental operating microscope) for the treatment.

After administration of local anesthesia and rubber dam isolation of the involved tooth ; access cavity was prepared using carbide bur and refined using ultrasonic tip in both groups. In both the groups similar protocol for irrigation, obturation and post operative restorations was followed. Immediate post-operative radiograph was taken using preset exposure parameters and follow up clinical and radiographic examination was carried at 12th month.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Double (Participant, Outcomes Assessor)

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Patient willing to participate in the study
  • •Age > 18 years
  • •Maxillary permanent first molar having apical periodontitis requiring primary endodontic treatment
  • •Radiographic evidence of periapical radiolucency (minimum size 2 mmx 2 mm) and a diagnosis of pulpal necrosis as confirmed by negative response to cold and electrical tests and absence of bleeding on entering the pulp chamber

Exclusion Criteria

  • •Unwillingness of patient.
  • •Retreatment cases
  • •Presence of internal or external resorption ,root canal perforations during endodontic treatment and immature teeth.
  • •Periodontally compromised teeth
  • •Immunocompromised, diabetic, pregnant and hypertensive patients
  • •Vertical root fractures
  • •Teeth those are not suitable for rubber dam application

Arms & Interventions

Experimental group

Experimental

Nonsurgical Root canal therapy was performed using dental operating microscope in the experimental group.

Intervention: Nonsurgical Root canal therapy (Procedure)

Experimental group

Experimental

Nonsurgical Root canal therapy was performed using dental operating microscope in the experimental group.

Intervention: Dental operating microscope (Device)

Control group

Active Comparator

Nonsurgical Root canal therapy was performed without any magnification aid in control group.

Intervention: Nonsurgical Root canal therapy (Procedure)

Outcomes

Primary Outcomes

Clinical and radiographic success

Time Frame: 12 months

long term clinical and radiographic success measured in terms of reduction in size of periapical radiolucency on radiograph from baseline to 12 months using PAI score 1,2 as healing and more than 2 as non healing

Secondary Outcomes

  • Number of canals located in MB root(12 months)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

Loading locations...

Similar Trials