SLM2204: Endodontic Treatment Using CTZ Paste in Primary Teeth

Sponsor
Faculty Sao Leopoldo Mandic Campinas (Other)
Overall Status
Unknown status
CT.gov ID
NCT03731975
Collaborator
(none)
174
1
2
29
6

Study Details

Study Description

Brief Summary

The aim of this study is to evaluate the efficacy of CTZ Paste in primary teeth, compared to endodontic treatment with Guedes-Pinto Paste. This is a multicenter, randomized, double-blind (patient), controlled and non-inferiority clinical study on 174 primary molars and 174 primary incisors of 3-6 years-old children with carious lesions with pulp involvement. The sample unit will be the tooth, which will be randomized into two groups. The teeth allocated to the experimental group will be treated with CTZ Paste, whereas the treatment of those teeth allocated to the control group will employ the Guedes-Pinto Paste. The procedures performed will be evaluated clinically and radiographically at 6 and 12 months. Secondary outcomes such as cost, discomfort, satisfaction and quality of life will also be evaluated.

Condition or Disease Intervention/Treatment Phase
  • Procedure: CTZ Paste
  • Procedure: GP Paste
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
174 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Participant, Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Efficacy of Endodontic Treatment Using CTZ Paste in Primary Teeth: Randomized Clinical Trial
Actual Study Start Date :
Jul 1, 2017
Actual Primary Completion Date :
Dec 1, 2018
Anticipated Study Completion Date :
Dec 1, 2019

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: CTZ Paste

Endodontic treatment with CTZ paste.

Procedure: CTZ Paste
Tooth allocated to this group will be treated with CTZ paste, according to the Cappielo's protocol (1964), updated by Moura et al. (2016).

Experimental: GP Paste

Endodontic treatment with Guedes-Pinto paste.

Procedure: GP Paste
Tooth allocated to this group will be treated with Guedes-Pinto paste, according to the Guedes-Pinto's protocol (1981), updated by Mello-Moura et al. (2011).

Outcome Measures

Primary Outcome Measures

  1. Clinical and radiographical efficacy of the endodontic treatment [12 Months]

    The tooth will be evaluated according to the presence of mobility (yes or no) and regarding radiolucency area on initial and final radiography (measured and compared with the program ImageJ).

Secondary Outcome Measures

  1. Cost-efficacy [Through study completion (12 months)]

    The costs of each treatment procedure will be calculated and compared with thresholds values for intervention cost-effectiveness by region, determined by World Health Organization (http://www.who.int/choice/costs/CER_levels/en/). These values will be combined with the evaluated efficacy of the treatments (according description of Outcome 1).

  2. Children's satisfaction with treatment [Through study completion (12 months)]

    The satisfaction of each treatment will be evaluated using the Wong-Baker Facial Scale (Wong & Baker, 1988). The patient will be asked to choose the face that is more similar to how he/she felt during the treatment. The answer should be given solely by the child, which means no parental or professional interferences.

  3. Parents/Guardians' satisfaction with children's treatment [Through study completion (12 months)]

    The parents' satisfaction with each treatment will be evaluated using the Parent's Questionnaire about Teeth Appearance (Furtado et al., 2012).

  4. Impact of treatment on children's quality of life [Baseline and 12 months]

    The oral health related quality of life will be measured using a validated questionnaire according to the children's age. The "Early Childhood Oral Health Impact Scale" (ECOHIS) (Tesch et al., 2008) will be applied with 4-5 years old patients. The "Child Perceptions Questionnaire" (CPQ) will be used for 6-9 years old patients (Martins et al., 2009). The same questionnaire will be applied immediately before the procedure and on 12 months follow-up. Only one type of questionnaire will be used with each child, according to its age.

Eligibility Criteria

Criteria

Ages Eligible for Study:
3 Years to 6 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • children aged from 3 to 6 years and 11 months;

  • children present at least one upper or lower molar or primary upper incisor with untreated carious lesion with pulp envelopment;

  • children assent to participate in the study through collaborative behavior;

  • children's parents/guardians consent to their participation by signing the Informed Consent Form (ICF).

Exclusion Criteria:
  • tooth with carious lesion involving three or more dental surfaces, making the restoration extremely difficult or impossible;

  • tooth with internal or external resorption in more than 1/3 of the root length;

  • tooth whose crypt of the successor permanent is affected;

  • tooth which have less than 2/3 of the root;

  • patients who present health problems with oral impairment.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Faculdade Sao Leopoldo Mandic Campinas SP Brazil 13045-755

Sponsors and Collaborators

  • Faculty Sao Leopoldo Mandic Campinas

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Jose Carlos P Imparato, Principal Investigator, Clinical Professor, Faculty Sao Leopoldo Mandic Campinas
ClinicalTrials.gov Identifier:
NCT03731975
Other Study ID Numbers:
  • SLM4
First Posted:
Nov 6, 2018
Last Update Posted:
Dec 24, 2018
Last Verified:
Dec 1, 2018
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Jose Carlos P Imparato, Principal Investigator, Clinical Professor, Faculty Sao Leopoldo Mandic Campinas

Study Results

No Results Posted as of Dec 24, 2018