Clinical Trials Logo

Clinical Trial Summary

Objective: Early loss of primary teeth due to caries, can cause occlusion disorders, aesthetic problems, nutritional problems, abnormal language habits, speech disorders and psychological problems temporary or permanent. The purpose of this study was to evaluate the success of using prefabricated aesthetic crowns for the restoration of excessive tooth loss. Study design: In this randomized, non-blinded clinical study a total of 45 teeth were included, primary molars and anterior teeth and requiring restoration after root canal treatment. Stainless steel(SCC), zirconia(ZC) and strip(S) crowns compared clinically, radiographically and periodontally during follow up period for 6 months. Parents were asked to fill out questionnaire at the 1st and 6th months to evaluate the satisfaction level. In addition, patients' pain and discomfort level was assessed using the visual analogue scale (VAS) scale.


Clinical Trial Description

The color of crowns made it impossible to blind during clinical assessment. Thus, this study was a non-blinded, randomised, and prospective clinical trial. Sample size: This study included 20 maxillary anterior and 25 posterior teeth that required restoration due to excessive material loss. The study groups were: Zirconia crown(ZC) restoration on the primary central and lateral tooth with root canal treatment (n = 10), strip crown(S) restoration on the primary central and lateral tooth with root canal treatment (n = 10), Zirconia crown(ZC) restoration on primary teeth with root canal treatment (n = 12), Stainless-steel crown(SSC) restoration on primary teeth with root canal treatment (n = 13). Clinical Procedure: Assessment Clinical assesment: Table 1 Gingival scores: Löe and Silness Gingival Index(GI)[Löe, 1967]. Periapical radiographic evaluation: Preoperative and every follow up visit. (Radiographic assesment: Table 2) Intraoral photos (standard method): before treatment, after treatment and at every follow-up visit. Crown restoration: All caries were removed after administration of local anaesthesia and proper isolation. Calcium hydroxide/iodoform paste (Vitapex®) pulpectomy was performed according to the guideline. Teeth were restored with a composite resin Nova Resin (IMICRYL®, Konya, Turkey) and glass ionomer cement (MERON®, Voco, Germany) was used as a base material. Strip Crown Forms (3M-ESPE, St. Paul,Minnesota, USA) were used to restore teeth group SC. ZC group (NuSmile, Houston, Tex. the USA) and SCC(3M ESPE, Minnesota, USA) used. Visual analogue scale(VAS): 0-2: no pain/discomfort 4-6:moderate 8-10: high pain/discomfort. The child was asked to choose his/her feelings about the tooth after the procedure and in follow-up appointments. Parents were asked to complete their satisfaction surveys, including the post-op and 6-month controls for patient satisfaction assessment. Statistical Method: IBM® SPSS® Statistics V23 analysed data. The Mann-Whitney U and Chi-square tests were used for intergroup comparisons within the anterior and posterior regions. The Friedman and Cochrane Q tests were used for intra-group time-wise comparisons. Analysis results were presented as the median (q1-q3) and frequency (percentage). P<0.05 was considered statistically significant. Table 1: Clinical assesment Crown retention 0= yes 1= no Individual modified gingival index 0= healthy 1= mild gingival bleeding with a papillus 2= severe inflammation Plaque index 0= no plaque 1. = presence of plaque as a film in the gingival margin 2. = presence of moderate plaque 3. = plaque covering a large number of surfaces Color change 0 = no coloring 1. = minor coloration 2. = noticeable coloration Buccal strip crown surface 0 = no loss 1 = less than 50% loss 2 = more than 50% loss 4 = loss of the entire surface Surface abrasion of the antagonist teeth 0= no abrasion 1. abrasion started on the incisal surface of the casps 2. abrasion more than on the casps Position of the crowns regarding gingival margin 0= subgingival 1= supragingival Occlusion 0= contact (marked or superficial) 1= no contact Condition of the antagonistic tooth 0= natural tooth 1. restored tooth 2. stainless steel crown 3. aesthetic crowns Location on the arch curve 0= normal alignment 1. with rotation 2. wrong position Proximal contacts 0= good (floss passing) 1= weak, no contact Table 2. Postoperative Radiographic Evaluation Criteria and Scores Radiographic evaluation of crown margins 0=good adaptation, continuity in crown contractions 1. small radiolucent area under the restoration 2. huge openings 3. loss of restoration Radiographic evaluation 0= healthy, no pathology 1. presence of a pathology that does not require immediate treatment 2. presence of pathology requiring immediate treatment Radiographic evaluation of pulpal treatment 0=appropriate root treatment 1. short or overflowed root treatment 2. failed pulpal treatment 3. tooth with no pulpal treatment ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04574180
Study type Interventional
Source TC Erciyes University
Contact
Status Completed
Phase N/A
Start date January 1, 2017
Completion date September 9, 2019

See also
  Status Clinical Trial Phase
Completed NCT03637309 - Multi-Media Parent-based Intervention to Promote Dental Hygiene Among Young Children: BeReady2Smile N/A
Completed NCT05531435 - Local Anesthesia With Computerized Device for Restorative Procedures in Pediatric Patients N/A
Recruiting NCT04538963 - Arrest of Proximal Caries Using Orthodontic Bands and Glass Ionomer Cement N/A
Not yet recruiting NCT05529433 - Pain Assessment During Chemo-Mechanical and Smart Burs Caries Removal Versus Atraumatic Restorative Treatment in Carious Primary Molars N/A
Completed NCT03063307 - Effectiveness of Silver Diamine Fluoride in Arresting Dental Caries N/A
Recruiting NCT05512156 - Toothbrushing Program in Saudi Arabia "TOPS" N/A
Not yet recruiting NCT06081868 - RCT on Effectiveness of Oral Health Preventive Programmes in School Children in Uganda N/A
Recruiting NCT06011005 - Efficacy of Ethyl Chloride Topical Anesthesia Application on the Pain Perception During Intra-oral Injections in Children in Comparison to Benzocaine Gel. N/A
Completed NCT05645029 - Evaluation of Glass Ionomer Cement Modified With Chlorhexidine and Titanium Dioxide in Primary Molars (RCT) N/A
Recruiting NCT04195386 - Efficacy of a Chemically Activated Composite Resin Alkasite in Atypical Caries Lesions of Deciduous Teeth N/A
Recruiting NCT04195022 - Comparison of a Chemically Activated Composite Resin Alkasite With Resin Composite in Atypical Caries Lesions of Deciduous Teeth N/A
Completed NCT03480516 - Comparison of Caries Arrested & Prevented Among SDF, NaF Varnish and Combination in Children N/A
Completed NCT03311438 - Oral Health Intervention Program for Children With Congenital Heart Defects N/A
Completed NCT05110534 - Supportive Caries Preventive Programme in Children Undergoing Dental General Anaesthesia N/A
Completed NCT05638217 - Efficacy of the Use of Silver Diamine Fluoride and Sodium Fluoride Varnish for the Treatment of Caries in Children
Completed NCT02002728 - Comparison of Early Caries Detection in Children Utilizing an Electrical Conductance Device and the Gold Standard of Visual-tactile Technique. N/A
Active, not recruiting NCT05121584 - Evaluation of Two Different Types of Zirconia Crowns Used in Carious Primary Anterior Teeth N/A
Completed NCT04666597 - Pandemic-adapted Caries Care Multicentre Single-group Interventional Study
Completed NCT05652231 - Assessment of Dental Caries Among a Group of Institutionalized Orphan Children Compared to Parented School Children
Completed NCT06018584 - Biostimulation After Tooth Extraction N/A