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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04144062
Other study ID # 318
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date November 25, 2019
Est. completion date February 20, 2021

Study information

Verified date February 2021
Source Minia University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

study aims to compare hybrid ceramic CAD/CAM and prefabricated zirconia crowns restoring primary molars through In-vivo evaluation of the clinical outcomes in terms of; treatment failure, amount of tooth wear in the opposing tooth and gingival health


Recruitment information / eligibility

Status Completed
Enrollment 120
Est. completion date February 20, 2021
Est. primary completion date February 20, 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 4 Years to 7 Years
Eligibility Inclusion Criteria: 1. Age range of the patients from 4 to 7 years old. 2. Have no history of spontaneous pain or swelling. 3. Patients willing to return for follow-up examinations and evaluation. 4. Medically free patients or with controlled systemic disease ASA I or II. 5. No active periodontal diseases. 6. Patients with posterior pulpotomized tooth/teeth indicated for crown restoration (e.g. 2-3mm of teeth above cement-enamel junction). Exclusion Criteria: 1. Age range of the patients from 4 to 7 years old. 2. Have no history of spontaneous pain or swelling. 3. Patients willing to return for follow-up examinations and evaluation. 4. Medically free patients or with controlled systemic disease ASA I or II. 5. No active periodontal diseases. 6. Patients with posterior pulpotomized tooth/teeth indicated for crown restoration (e.g. 2-3mm of teeth above cement-enamel junction).

Study Design


Related Conditions & MeSH terms

  • Restoration of Primary Molars With CAD/CAM Crowns

Intervention

Other:
CAD/CAM crowns
CAD/CAM crowns

Locations

Country Name City State
Egypt Ahmad Elheeny Minya

Sponsors (1)

Lead Sponsor Collaborator
Ahmad Elheeny

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary clinical success United States Public Health Service (USPHS) index 1 year