Erciyes University
Kayseri, 38039, Turkey (Türkiye)
NCT Number: NCT04574180
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.
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Notify Me3 year–11 year
All sexes
Interventional
Not applicable
Kayseri, 38039, Turkey (Türkiye)
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
Color change 0 = no coloring
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
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
Location on the arch curve 0= normal alignment
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
Radiographic evaluation 0= healthy, no pathology
Radiographic evaluation of pulpal treatment 0=appropriate root treatment
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Pediatric size dental crown; restore damaged tooth to its normal shape, size, and function.
Other names: Zirconia Crown (NuSmile, Houston, Texas, USA), Stainless Steel Crown (3M-ESPE, St. Paul, Minnesota, USA), Strip Crown (3M-ESPE, St. Paul, Minnesota, USA)
Time frame: 6 months follow up period
The incidence of crown retention, gingival index, marginal crown localisation
Time frame: 6 months follow up period
Periapical film: the rate of radiolucency. According to the index, each tooth was categorized as having a normal periapical structure (score 1), small changes in bone structure (score 2), changes in bone structure with some mineral loss (score 3), periodontitis with well-defined radiolucent areas (score 4), or severe apical periodontitis with exacerbating features (score 5)
Time frame: 6 months follow up period
A Visual Analogue Scale (VAS): no pain (0-4 mm), mild pain(5-44 mm), moderate pain (45-74 mm), and severe pain (75-100 mm)
TC Erciyes University
Other
Can Zirconia Crown be the First Restorative Choice After Endodontic Treatment for Primary Teeth?
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