Status:
UNKNOWN
Retention of Flowable Resin With Sprg and of a Flowable Resin in First Permanent Molars
Lead Sponsor:
Catherine Christie Ruiz Yasuda
Conditions:
Pit and Fissure Sealant
Eligibility:
MALE
6-8 years
Phase:
NA
Brief Summary
Objective: Determine which of the two sealants has better retention during the periods of 6, 9 and 12 months, one based on flowable resin with sprg or the other only based on flowable resin and we hav...
Detailed Description
The following research project is being carried out following the 2010 Consort Declaration (32) 1. Ethical considerations: Declaration of Helsinki. Access to the data of the research subjects in orde...
Eligibility Criteria
Inclusion
- Children whose parents accepted their participation in the study and who signed the Informed Consent (Annex 1)
- Children enrolled in the school of the district of Pichanaki, province of Chanchamayo and department of Junín
- Children between 6 and 8 years, with permanent upper and / or lower molars with the following characteristics:
- Deep cavities and cavities free of cavities, rated 0 and 1 according to ICDAS II Non-cavitated caries in enamel C1 according to ICDAS II Green and Vermillion Simplified Oral Hygiene Index (OHS) of 1 Have a pair of non-cavitated caries-free counterparts.
- Collaborative and receptive children.
Exclusion
- Children with the presence of a deep dental caries lesion, with pulp exposure, history of pain and presence of fistula or abscess adjacent to decayed tooth.
- Medically compromised children
- Children with developmental enamel defects.
- Children with a known allergy to any of the resins used
- Children with previously placed sealants or restorations
- Children with bruxism or malocclusion
- Children residing outside the city.
- Children with poor hygiene
- Criteria for withdrawal of research subjects
- When they did not attend the evaluations
- If the participant has partial retention and total loss of the sealant, he will be withdrawn from the study after placing a new sealant.
- If a patient moves to another region, it will be grounds for withdrawal from the study.
- If the patient wishes to leave the study, they are considered outside the study
- Criteria for termination or interruption of the clinical trial.
- When the 12-month follow-up of all the recruited patients, excluding the withdrawn ones, is completed, the study will be terminated.
- Work is interrupted
Key Trial Info
Start Date :
March 1 2021
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
August 1 2022
Estimated Enrollment :
60 Patients enrolled
Trial Details
Trial ID
NCT04701294
Start Date
March 1 2021
End Date
August 1 2022
Last Update
January 8 2021
Active Locations (1)
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1
Manuel Gonzales Prada School
Alto Pichanaki, Chanchamayo, Peru