The use of therapeutic paracetamol ice cream in the postoperative period of children: a randomized clinical trial

Not Applicable

• Conditions: Postoperative Care; Oral Surgery; Pediatric Dentistry; Pharmacology; Other specified diseases of the jaws; K10.8; E04.545.700; E06.892; H02.163.876.600; H01.158.703

• Registration Number: RBR-992839
• Lead Sponsor: Centro Universitário Luterano De Palmas - CEULP/ULBRA

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2020-06-23
• Last Update Posted: 29 May 2023

Recruitment & Eligibility

• Status: ot yet recruiting
• Sex: Not specified
• Target Recruitment: Not specified

Inclusion Criteria

Children aged 6 to 12 years; Conditioned children (collaborators); Children with indication of extraction on any deciduous or permanent teeth; Of both sexes (male and female); Children who have signed the free and informed consent term (TALE ); Children whose legal guardian has signed the informed consent form (ICF)

Exclusion Criteria

Children with sensitivity to the components of the paracetamol / ice cream formulation; Children under 6 years of age; Children with lactose intolerance.; Children with cognitive development disorders; Children with heart disease; Children with liver disease; Children with kidney disease; Children with coagulopathy; Children with diabetes; Children unaccompanied by their legal guardian.

Study & Design

• Study Type: Intervention
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
It is believed that children who use the therapeutic ice cream emulsion formula of paracetamol will have less pain and less bleeding compared to ice cream without the addition of paracetamol in the postoperative period of tooth extractions.<br>

Secondary Outcome Measures

Name	Time	Method
Children are expected to have greater adherence to therapeutic treatment in the postoperative period