Clinical Trials Logo

Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT06113770
Other study ID # 787/4375
Secondary ID
Status Active, not recruiting
Phase N/A
First received
Last updated
Start date May 1, 2023
Est. completion date December 2023

Study information

Verified date November 2023
Source Al-Azhar University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

, in this studythe investigator will compare between ready-made zirconia crowns and Computer-aided design and Computer-aided manufacturing (CAD/CAM) polymethyl methacrylate (PMMA) crowns to overcome the disadvantages of ready-made zirconia crowns.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 17
Est. completion date December 2023
Est. primary completion date November 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 4 Years to 8 Years
Eligibility A- Inclusion Criteria: 1. Primary molars indicated for crown restoration (pulp treated molars indicated for crown 2. Co-operative child (Frankel scale +ve and ++ve) 3. The age ranged from 4 to 8 years regardless of sex or socioeconomic background. B- Exclusion Criteria:- 1. Badly decayed non-restorable tooth indicated for extraction. 2. Patients with parafunctional habits like bruxism. 3. Systemic diseases with oral manifestation or blood diseases.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
preparation of the tooth to receive ready made zirconia crown
Occlusal reduction 1 to 2 mm using flame bur . Open the interproximal contacts. The tooth should be reduced circumferentially by approximately 0.5-1.5mm . The preparation margin should be carefully extended and refined to a feather-edge approximately 1-2mm subgingivally . Crown size will be determined using try in kit .
preparation of the tooth to receive CAD CAM PMMA custom made crown
Open the interproximal contacts . The tooth should be reduced circumferentially by approximately 0.5-1mm . The preparation margin should be carefully extended and refined to a feather- edge approximately 1-2mm subgingivally . Rubber base impression will be taken by BMS additional silicone kit to the prepared tooth and will be sent to the laboratory to be scanned and to design the crown . The final crown will be cemented using glass ionomer cement .

Locations

Country Name City State
Egypt AlAzharU Cairo

Sponsors (1)

Lead Sponsor Collaborator
Adel Sherif Mostafa Rehab

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary Gingival condition Löe & Silness gingival index in 6 months
Secondary gingival bleeding Papilla Bleeding Index 6 months
See also
  Status Clinical Trial Phase
Completed NCT03290625 - Intranasal Sedation With Dexmedetomidine and Ketamine in Pediatric Dentistry (NASO II) Phase 4
Completed NCT06003257 - Comparison Between Stainless-Steel, Zirconia and Fiberglass Crowns for Deciduous Molars N/A