Skip to main content
Clinical Trials/NCT03423329
NCT03423329
Completed
Not Applicable

Effect of Preoperative Oral Administration of Ibuprofen and Acetaminophen on the Anesthetic Efficacy of Buccal Infiltration During Vital Pulpotomy of Mandibular Primary Molars: A Prospective, Double-blinded, Randomized Controlled Trial

Ain Shams University1 site in 1 country60 target enrollmentJanuary 20, 2018

Overview

Phase
Not Applicable
Intervention
Brufen
Conditions
Anesthesia, Local
Sponsor
Ain Shams University
Enrollment
60
Locations
1
Primary Endpoint
Pain/discomfort felt during vital pulpotomy of mandibular second primary molars
Status
Completed
Last Updated
7 years ago

Overview

Brief Summary

This Randomized study was designed to assess and compare the effect of two analgesic premedications (Ibuprofen BP 100 mg/5 ml and Paracetamol 200 mg/5ml.) on the anesthetic efficacy of buccal infiltration in vital pulpotomy of primary mandibular molars in children . A multivitamin with the same color as the twp tested medications will be administered to children in the control group. Parents of eligible children will be informed about the nature of the procedure, the purpose of the study, any possible discomfort or risks and a signed informed consent will be obtained from them prior to enrollment.

Detailed Description

A total of 60 healthy children will be recruited from the outpatient clinic of the Pediatric Dentistry and Dental Public Health Department, Faculty of Dentistry, Ain Shams University. Inclusion Criteria include: age group 7-9 years Without systemic or mental disorders. Who could be categorized as cooperative according to Wright's classification for child behavior Ability of child to understand the use of pain scales; Having at least one lower second primary molar with deep caries indicated for pulpotomy; Absence of any periapical or furcation radiolucency on radiographs, Absence of any signs of internal or external resorption on radiographs, A vital coronal pulp on access opening. . Patients who had taken analgesics within 12 hours before administration of the study drugs or those having active pain, pulpitis or abscess related to the designated mandibular molar will not be included. To ensure randomization and allocation concealment, children will be randomly assigned to the three groups using computer-generated numbers. One operator will do pulpotomy for all participants and to ensure blinding, another author ( will give the premedication to children.Pain during pulpotomy will be assessed using Wong Baker FACES pain assessment tool.

Registry
clinicaltrials.gov
Start Date
January 20, 2018
End Date
April 25, 2018
Last Updated
7 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Reham Abou El Fadl

Principal investigator

Ain Shams University

Eligibility Criteria

Inclusion Criteria

  • age group 7-9 years
  • Patients medically free.
  • Patients who can be categorized as cooperative or potentially cooperative according to Wright's classification for child behavior
  • Patients able to understand the use of pain scales;
  • Having at least one lower second primary molar with deep caries indicated for pulpotomy;
  • A vital coronal pulp on access opening of designated molar.

Exclusion Criteria

  • Patients with allergic reactions, sensitivity, or contraindications to any tested drugs
  • Patients who had taken analgesics within 12 hours before administration of the study drugs
  • Patients having active pain, pulpitis or abscess related to the designated mandibular molar.
  • Children with special health care needs or any systemic problems
  • Presence of periapical or furcation radiolucency on radiographs in relation to designated molar
  • Presence of of any signs of internal or external resorption on radiographs in relation to designated molar

Arms & Interventions

Group A

Intervention:Drug: Brufen \& Placebo Brufen syrup 10 ml, once, 1 hour before local anesthesia

Intervention: Brufen

Group A

Intervention:Drug: Brufen \& Placebo Brufen syrup 10 ml, once, 1 hour before local anesthesia

Intervention: Placebo for Brufen

Group B

Intervention: Drug: Cital and Placebo Cital Syrup 10 ml, once 1 hour before Local anesthesia

Intervention: Cital

Group B

Intervention: Drug: Cital and Placebo Cital Syrup 10 ml, once 1 hour before Local anesthesia

Intervention: Placebo for Brufen

Group C

Intervention: Drug: Placebo Other names: (Placebo for Brufen) (Placebo for Cital) Sansovit Iron Multivitamin syrup, an orange-coloured, orange-flavoured

Intervention: Brufen

Group C

Intervention: Drug: Placebo Other names: (Placebo for Brufen) (Placebo for Cital) Sansovit Iron Multivitamin syrup, an orange-coloured, orange-flavoured

Intervention: Cital

Group C

Intervention: Drug: Placebo Other names: (Placebo for Brufen) (Placebo for Cital) Sansovit Iron Multivitamin syrup, an orange-coloured, orange-flavoured

Intervention: Placebo for Brufen

Outcomes

Primary Outcomes

Pain/discomfort felt during vital pulpotomy of mandibular second primary molars

Time Frame: 75 minutes after drug administration

Using Wong Baker FACES pain assessment tool Children will be asked to rate any pain felt during coronal access

Study Sites (1)

Loading locations...

Similar Trials