Checking Occlusion During Stainless Steel Crown Placement

Sponsor
Riyadh Colleges of Dentistry and Pharmacy (Other)
Overall Status
Completed
CT.gov ID
NCT02437565
Collaborator
(none)
60
1
2
20
3

Study Details

Study Description

Brief Summary

Stainless steel crowns are arguably the most successful posterior restorations in primary teeth and have been so for more than 50 years. Stainless steel crowns offer durability and success rates in excess of 95% making them the restoration of choice for posterior primary teeth in children treated under general anesthesia.

Failures of stainless steel crowns placed on primary teeth have been documented using several criteria including marginal adaptation, recurrent caries, abscess formation or root resorption, loss of the crown due to faulty retention and even perforation of the crown . Despite the probability that factors such as root resorption and failure of endodontic treatment could be due to traumatic occlusion, surprisingly little evidence is available in literature on the attempts made to check or evaluate the occlusion of stainless steel crowns placed under general anesthesia The aim of this study was to compare the time taken for placement and the overall success of bilateral multiple stainless crowns placed under general anesthesia using an occlusal index and compare them to crowns placed without such an index, using a randomized control study design

Condition or Disease Intervention/Treatment Phase
  • Other: Stainless steel crown
  • Other: Occlusal Template
N/A

Detailed Description

A total of 60 patients (32 male and 28 female) aged between 4 and 7 years (Mean age 4.8 years, SD +/- 1.09 years) who met the inclusion criteria were recruited after obtaining informed consent from the parent. No financial incentives were offered for participation in the study. A total of 51 (29 male and 22 female) patients completed the six month follow up requirement (Fig 2).

Evaluation Crowns and the Procedure All patients were evaluated at 24 hours, one week, three months and six months post-operatively. Clinical criteria evaluated included the reporting of pain, discomfort, difficulty in mastication or high points reported by the patient. Tenderness on percussion, presence of premature mobility and clinical evidence of an abscess or fistula were checked by one of the investigators (SCP). Periapical digital radiographs were taken using a digital sensor (Schick Elite, Sirona Dental Inc. Long Island NY. USA) and were evaluated by the same examiner for radiographic evidence of failure. In order to ensure blinding the investigator (SCP) recording the findings was not made aware of which group the patient belonged to. The time taken for each procedure was calculated from the time of placement of the throat pack to the time of removal of the throat pack and was obtained from the intra-operative anesthesiologist notes. If failure of the crown occurred at 3 months, these teeth were excluded from the 6 month evaluation.

Statistical Analyses The parametric values of the control and case groups were compared using the student's t test. The non-parametric values of the control and case groups were compared using the Mann Whitney U test. All tests were conducted at p value of 0.05

Study Design

Study Type:
Interventional
Actual Enrollment :
60 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Participant, Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Checking Occlusion During Stainless Steel Crown Placement in Children Under General Anesthesia - Evaluation of a Novel Technique
Study Start Date :
Aug 1, 2013
Actual Primary Completion Date :
Jan 1, 2015
Actual Study Completion Date :
Apr 1, 2015

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Control

Placement of stainless steel crown under general anesthesia without the use of an occlusal template

Other: Stainless steel crown
Placement of stainless steel crowns for teeth that have undergone pulpotomy for the treatment of pulpitis induced by severe early childhood caries under general anesthesia

Experimental: Impression

Placement of stainless steel crown under general anesthesia with the use of an occlusal template prepared after making an impression of the teeth using a fast setting polyvinyl siloxane material

Other: Stainless steel crown
Placement of stainless steel crowns for teeth that have undergone pulpotomy for the treatment of pulpitis induced by severe early childhood caries under general anesthesia

Other: Occlusal Template
Use of an occlusal template for the placement of stainless steel crowns under general anesthesia

Outcome Measures

Primary Outcome Measures

  1. Time taken for the completion of oral rehabilitation [Measured at the end of the clinical procedure]

    Time taken for the completion of oral rehabilitation under general anesthesia

Secondary Outcome Measures

  1. Discomfort on Biting [up to 6 months]

    Patient complains of discomfort on biting

  2. Radiographic Evidence of Abscess [up to 6 monhts]

    Presence of abcess on a periapical radiograph

  3. Dislodgement of crown [up to 6 months]

    Loss of retention of the crown resulting in the dislodgement or complete removal of crown

Eligibility Criteria

Criteria

Ages Eligible for Study:
4 Years to 7 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Clinical Diagnosis of Severe Early Childhood Caries

  • Have behavioral problems that require management under general anesthesia

  • ASA class I

  • Deep Dental Caries involving the pulp in all eight primary molars

Exclusion Criteria:
  • ASA class II or above

  • Initial treatment plan cannot be carried out

  • Need for extraction or pulpectomy in one or more primary molar

Contacts and Locations

Locations

Site City State Country Postal Code
1 Riyadh Colleges of Dentistry and Pharmacy Riyadh Saudi Arabia

Sponsors and Collaborators

  • Riyadh Colleges of Dentistry and Pharmacy

Investigators

  • Principal Investigator: Sharat C Pani, MDS, Riyadh Colleges of Dentistry and Pharmacy

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Dr Sharat Pani, Assistant Professor, Pediatric Dentistry, Riyadh Colleges of Dentistry and Pharmacy
ClinicalTrials.gov Identifier:
NCT02437565
Other Study ID Numbers:
  • FRP/2013/046
First Posted:
May 7, 2015
Last Update Posted:
May 7, 2015
Last Verified:
May 1, 2015
Additional relevant MeSH terms:

Study Results

No Results Posted as of May 7, 2015