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Clinical Trials/NCT03493321
NCT03493321
Unknown
Not Applicable

Role of PRF With MTA and Theracal After Pulpotomy in Relieving Pain and Maintaining the Vitality of the Remaining Radicular Pulp Tissue in Permanent Posterior Teeth With Closed Root Apices: "Randomized Controlled Trial"

Cairo University0 sites98 target enrollmentAugust 22, 2019
ConditionsNeuritis

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Neuritis
Sponsor
Cairo University
Enrollment
98
Primary Endpoint
pain after the process
Last Updated
6 years ago

Overview

Brief Summary

this research will evaluate the effect of PRF with different bioactive materials in dentistry

Detailed Description

PRF will be used with MTA and Theracal to evaluate its effect upon these materials in reliving pain and maintains the teeth vitality in permanent teeth with closed apices, in order to improve the materials outcome.

Registry
clinicaltrials.gov
Start Date
August 22, 2019
End Date
September 30, 2019
Last Updated
6 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Sarah Essam

Principle investigator

Cairo University

Eligibility Criteria

Inclusion Criteria

  • Patients suffering from Symptomatic pulpitis.
  • Patients should be free from any systemic disease that may affect normal healing and predictable outcome.
  • Patients who will agree to the consent and will commit to follow-up period.
  • Patients with mature root.
  • Patients with no periapical lesion.
  • Patients with localized pain.
  • Posterior teeth only will be involved

Exclusion Criteria

  • Patients with immature roots.
  • Patients with any systemic disease that may affect normal healing.
  • Patients with periapical lesions or infections.
  • Pregnant females.
  • Patients who could/would not participate in a 1-year follow-up.
  • Patients with fistula.
  • Patients with necrotic pulp.
  • Patients with old age.

Outcomes

Primary Outcomes

pain after the process

Time Frame: 1 year

Questionnaire by asking the patient about the pain intensity

Secondary Outcomes

  • no periapical radiolucency(1 year)
  • dentin bridge formation(1 year)

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