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Clinical Trials/NCT04133181
NCT04133181
Unknown
Not Applicable

Clinical and Radiographic Success of Guided Versus Conventional Periapical Endodontic Surgery: A Randomized Controlled Trial

Cairo University0 sites26 target enrollmentDecember 2019

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Endodontic Disease
Sponsor
Cairo University
Enrollment
26
Primary Endpoint
Clinical success
Last Updated
6 years ago

Overview

Brief Summary

This study is to compare the clinical and radiographic outcomes after guided periapical endodontic surgery versus conventional endodontic surgery.

Detailed Description

The aim of this study is to compare the clinical and radiographic outcomes after guided periapical endodontic surgery versus conventional endodontic surgery. Patients having mandibular posterior teeth indicated for endodontic surgery will be selected. Full medical and dental history will be obtained from all patients. Patients will be randomly assigned to either guided endodontic surgery or conventional endodontic surgery. Surgical procedures will be done under magnification. Root-end cavities will be filled using MTA.Post surgical instrucions will be given to patients. Surgical time will be recorded. Clinical and radiographic success will be asses at 6 and 12 month.

Registry
clinicaltrials.gov
Start Date
December 2019
End Date
October 2021
Last Updated
6 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

ahmed meneisy

Doctor Degree candidate

Cairo University

Eligibility Criteria

Inclusion Criteria

  • Patients in good general health.
  • Patients with age ranging between 18-50 years with no sex predilection.
  • Posterior teeth with an indication for endodontic surgery.
  • Patients' acceptance to participate in the study.

Exclusion Criteria

  • Patients with allergy to materials or medications used in the trial.
  • Pregnant female patients.
  • Teeth with pathoses associated with vertical root fracture.
  • Severe periodontal bone loss detected with a periodontal probe (5 mm probing depth).

Outcomes

Primary Outcomes

Clinical success

Time Frame: 1 year

Clinical assessment using a scale by friedman et al 2005 (healed, healing and persisting disease) which healed mean absence of clinical signs and symptoms, persisting disease mean presence of clinical signs and symptoms

Radio graphic Success

Time Frame: 1 year

Radiograhic assessment using a scale by friedman et al 2005 (healed, healing and persisting disease) which healed mean radiographic classification of complete healing or incomplete healing, persisting disease mean radiographic classification of unsatisfactory healing.

Secondary Outcomes

  • Time of surgery(During surgery)

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