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Evaluating the Efficiency of Newly Designed Prefabricated PMMA Crowns for Restoring Primary Teeth in Comparison to Stainless Steel and Zirconia Crowns

A

Ain Shams University

Status

Completed

Conditions

Decay, Dental

Treatments

Other: PMMA crowns

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

Evaluation of PMMA pediatric crowns

Full description

The aim of the present study is to evaluate the PMMA crowns regarding the following aspects:

I. Clinical evaluation of PMMA crowns regarding wear of opposing teeth when compared to zirconia crowns and stainless steel crowns after 6 months, and 12 months.

II. Color stability of PMMA crowns and zirconia crowns after 6 months, and 12 months.

III. Gingival health of restored teeth after 6 months, and 12 months. IV. Patient's satisfaction regarding the appearance and clinical performance of PMMA crowns when compared to stainless steel crowns and zirconia crowns through a given questionnaire.

Enrollment

20 patients

Sex

All

Ages

5 to 8 years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

  • Children included in the study should conform to the following criteria:

    1. Aged 5-8 years old

    2. Medically free

    3. Patient should suffer from extensively decayed primary lower second molar that will undergo pulpotomy.

    4. The anticipated exfoliation date of the selected primary teeth has to be more than 12 months from the date of the study start.

      Exclusion Criteria:

      Children with the following criteria will be totally excluded from the study:

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    1. Children who are extremely uncooperative and difficult to manage.
    2. Children suffering from any medical conditions that can't be managed in the clinic.
    3. Teeth with decay extending beneath the free gingival margin.
    4. Teeth that were grossly broken down, that cannot be restored.
    5. Presence of uncontrolled bleeding.
    6. Clinical or radiographic evidence of non-vitality such as presence of an abscess or a sinus, obvious discoloration, and premature hypermobility.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

20 participants in 3 patient groups

Stainless steel crowns
Active Comparator group
Description:
3M ESPE
Treatment:
Other: PMMA crowns
Zirconia crowns
Experimental group
Description:
Nu Smile
Treatment:
Other: PMMA crowns
PMMA crowns
Experimental group
Description:
Dental Direkt
Treatment:
Other: PMMA crowns

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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