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Comparative study of pre-medication with paracetamol, Ibuprofen and placebo on post operative pain following pulpotomy in 6-12 years old childre

Not Applicable
Recruiting
Conditions
Pulpotomy.
Inflammation of the dental pulp, usually due to bacterial infection in dental caries, tooth fracture, or other conditions causing exposure of the pulp to bacterial invasion. Chemical irritants, thermal factors, hyperemic changes, and other factors may als
K04.0
Registration Number
IRCT20221011056145N1
Lead Sponsor
Rasht University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
27
Inclusion Criteria

The children be 6-12 years old
Each patient must have at least 3 teeth for Pulpotomy and SSC in lower jaw
Parents' consent to perform the treatment

Exclusion Criteria

Not reaching hemostasis
Not reaching adequate anesthesia
Any kind of systemic disease that is in contrast to conservative pulp treatment
Any radiographic findings including:internal and external resorption, PDL Widening,furcation and periapical radiolucency,root canal calcification
Patients with any history of allergy to analgesics or any drugs used in the study
Patients are not reachable through phone call
Patients with Gastrointestinal problems, Favism, GERD,Active asthma
Patients with prolonged bleeding history
Presence of abscess or sinus tract

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Examining the type of drug on pain after pulpotomy treatment. Timepoint: The treatments are done with an interval of one week, and the child is asked to paint the face that is most similar to his feeling about the treated tooth in the intervals of 24, 48, 72 hours after the treatment. Method of measurement: comparative investigation of pre-treatment with paracetamol, ibuprofen and placebo on pain after pulpotomy treatment in children 6-12 years old the way of measuring the outcome variable is Wong-Baker scale.;Examining the age variable on pain after treatment. Timepoint: In the initial treatment session, the age is asked and recorded for each child. Method of measurement: In the initial treatment session, the age is asked and recorded for each child.;Examining the gender variable on pain after treatment. Timepoint: In the initial treatment session, the gender of the child is asked and noted. Method of measurement: In the initial treatment session, the gender of the child is asked and noted.
Secondary Outcome Measures
NameTimeMethod
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