Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT06003257
Other study ID # 286/2020
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date March 23, 2022
Est. completion date May 13, 2023

Study information

Verified date June 2023
Source Suez Canal University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The study will be divided into two parts: In vivo part and in vitro part.In vivo part: It will be a randomized clinical trial using split mouth technique on 44 primary molars in children aged from 4-8 years old selected from outpatient clinic of Department of Pediatric Dentistry, Faculty of Dentistry, Suez Canal University. The selected primary molars will be divided randomly into two main groups ,each group will be subdivided into two subgroups according to types of crowns that will be used as follows:- Group I:- comprise of 22 primary molars that will be subdivided into two subgroups, subgroup IA:-includes 11 primary molars will be restored by stainless steel crowns and subgroup IB:-includes 11 primary molars will be restored by zirconia crowns, Group II:- comprise of 22 primary molars that will be subdivided into two subgroups, subgroup IIA:-includes 11 primary molars will be restored by stainless steel crowns and subgroup IIB:-includes 11 primary molars will be restored by fiberglass crowns. The three types of crowns will be evaluated at the baseline once after cementation of the crowns and after one week,1 ,3,6,9 and 12 months follow up by using the following methods modified United States Public Health Service criteria, in terms of color match, marginal integrity, secondary caries and crown fracture, the gingival marginal status and parental satisfaction. In vitro part: It will be carried out on 30 mandibular primary molars, 15 mandibular first primary molars for microleakage test and 15 mandibular second primary molars for crown fracture resistance test for three crowns types.


Description:

The study will be a randomized clinical trial using split mouth technique on 44 primary molars in children aged from 4-8 years old selected from outpatient Clinic of Department of Pediatric Dentistry, Faculty of Dentistry, Suez Canal University after approval of Research Ethics Committee (REC) of the Faculty of Dentistry, Suez Canal University. The children participants and legal guardian of each participant will be assigned on informed consent of treatment procedures they will receive. A total of 44 primary molars will be included in this study using split mouth technique to ensure equalizing variables for both groups. The selected primary molars will be divided randomly into two main groups, each group will be subdivided into two subgroups according to types of crowns that will be used as follows: - - Group I: comprise of 22 primary molars that will be subdivided into two subgroups: - Subgroup IA: includes 11 primary molars will be restored by stainless steel crowns. - Subgroup IB: includes 11 primary molars will be restored by zirconia crowns. - Group II: comprise of 22 primary molars that will be subdivided into two subgroups: - Subgroup IIA: includes 11 primary molars will be restored by stainless steel crowns. - Subgroup IIB: includes 11 primary molars will be restored by fiberglass crowns. II.4 Clinical Procedures: - Eligibility criteria will be verified after the clinical and periapical radiographic examination. - The selected primary molars will be anesthetized to reduce discomfort during preparation. - Tooth preparation and crown cementation will be performed for each tooth according to the manufacture's instruction for each type of crowns. II.5 Methods of evaluation: The evaluation of each crown will be assessed at the baseline once after cementation and after one week,1, 3, 6,9 and 12 months follow up by using the following methods: II.5.1 Modified United States Public Health Service (USPHS) criteria: Modified United States Public Health Service (USPHS) criteria will be used in terms of marginal integrity, secondary caries, color match, and crown fracture


Recruitment information / eligibility

Status Completed
Enrollment 44
Est. completion date May 13, 2023
Est. primary completion date March 28, 2023
Accepts healthy volunteers No
Gender All
Age group 4 Years to 8 Years
Eligibility Inclusion Criteria: - 1. Apparently healthy children free from any systemic diseases. 2. Patient within the age group of 4 to 8 years old of both sexes. 3. Cooperative patient. 4. Patient with at least two bilateral primary molars indicated for full coverage as follows: 1. Multi-surfaces caries more than two surfaces 2. Pulp therapy treated primary molars 3. Developmental defects on tooth surface 4. Root resorption less than/ equal to1/3rd of root length 5. Parent willing to participate in the study. Exclusion Criteria: - Patient with primary molars have the following criteria: 1. Acute infection 2. Infra-occlusion 3. Mobility 4. Internal root resorption 5. Exfoliation imminent

Study Design


Related Conditions & MeSH terms


Intervention

Other:
stainless steel crown
stainless steel full coverage crown for deciduous teeth
zirconia crown
zirconia full coverage crown for deciduous teeth
fiberglass crown
fiberglass full coverage crown for deciduous teeth

Locations

Country Name City State
Egypt faculty of dentistry Suez canal university Ismailia

Sponsors (1)

Lead Sponsor Collaborator
Suez Canal University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary clinical performance " marginal integrity, color change, secondary caries and crown fractures" Modified United States Public Health Service (USPHS) criteria will be used in terms of marginal integrity, secondary caries, color match, and crown fracture immediately after cementation, after 1 month, 3 months, 6 months, 9 months and 12 months
Secondary Measuring of gingival marginal status The gingival marginal status will be assessed by the plaque index (PI) and gingival index where 0 normal gingiva and no plaque while 3 severe inflammation and abudance of soft matter within gingival pocket immediately after cementation, after 1 month, 3 months, 6 months, 9 months and 12 months
Secondary Measuring of parental satisfaction Parental satisfaction will be evaluated on a five-point Likert scale, which responders specify their level of satisfaction. parents will ask to rate parameters such as the crown's shape, size, color, and their overall satisfaction by using Parental satisfactions questionnaire immediately after cementation, after 1 month, 3 months, 6 months, 9 months and 12 months
See also
  Status Clinical Trial Phase
Completed NCT03290625 - Intranasal Sedation With Dexmedetomidine and Ketamine in Pediatric Dentistry (NASO II) Phase 4
Active, not recruiting NCT06113770 - Clinical Evaluation of Polymethyl Methacrylate CAD/CAM Crowns Versus Prefabricated Zirconia Crowns in Primary Molars N/A