Actively Recruiting

Phase Not Applicable
Age: 18Years - 40Years
All Genders
Healthy Volunteers
NCT06231290

The Influence of Magnification and Clinical Experience on the Outcome of Pulpotomy in Mature Adult Teeth

Led by Al-Azhar University · Updated on 2024-05-14

68

Participants Needed

1

Research Sites

66 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The goal of this interventional randomized clinical trial is to test the effect of magnification and clinical experience of the operator on the success rate of full pulpotomy in mature adult molar teeth. The main questions it aims to answer are: * Does the use of magnification raise the success rate of full pulpotomy of mature adult molars? * Does the clinical experience of the operator dentist raise the success rate of full pulpotomy of mature adult molars? Participants will be asked to do the following: * Receive the pulpotomy treatment of their target molar tooth. * Record the pain score in the pain assessment chart. * Attend the follow-up visits. They'll receive a full pulpotomy treatment of their target molar tooth. Researchers will evaluate the usage of magnification in performing the pulpotomy procedure of adult molar teeth by postgraduate or undergraduate operators in comparison to performing the same pulpotomy procedure without magnification to see if it raises the overall success rate of pulpotomy.

CONDITIONS

Official Title

The Influence of Magnification and Clinical Experience on the Outcome of Pulpotomy in Mature Adult Teeth

Who Can Participate

Age: 18Years - 40Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Healthy patients diagnosed with acute irreversible pulpitis related to maxillary or mandibular permanent molar teeth without apical periodontitis.
  • Age between 18 and 40 years.
Not Eligible

You will not qualify if you...

  • Non-vital teeth.
  • Immature teeth.
  • Presence of swelling or sinus tract.
  • Teeth with mobility grade II or III.
  • Immunocompromised patients.
  • Non-restorable teeth.
  • Teeth with apical periodontitis seen in periapical radiograph.
  • Periodontally affected teeth.
  • Teeth with reversible pulpitis.
  • Extensive non-stoppable bleeding more than 6 minutes.
  • Teeth with partial necrosis.

AI-Screening

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Trial Site Locations

Total: 1 location

1

Faculty of Dental Medicine, Al-Azhar University

Cairo, Egypt, 11751

Actively Recruiting

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Research Team

M

Mohamed A. Yahia, BSc

CONTACT

M

motaz M. Elsadat, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

4

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