The Efficacy of Analgesic Buffering With Sodium Bicarbonate for the Pediatric Dental Patient

Sponsor
University of Colorado, Denver (Other)
Overall Status
Withdrawn
CT.gov ID
NCT01883232
Collaborator
(none)
0
1
2
30
0

Study Details

Study Description

Brief Summary

As a dentist, administering anesthetic to patients, especially children, proves to be one of the most difficult parts of a procedure. Pain is one of the most common symptom in dentistry, and a serious concern for the dentist. The pain of the local anesthetic injection has several causes. Of the many reasons for pain at the site of injection, the acidity of the solution is thought to be most important. This study will be measuring the effects of adding sodium bicarbonate (buffer) to local anesthetic during dental procedures. This is commonly used in medical applications but is not widely used in the dental setting. Using this biochemistry and human physiology, one can predict when buffering the lidocaine injection, a quicker response in analgesia and a decrease in pain during administration. I will be measuring the effect using several measuring devices to gauge if buffering the local anesthetic will benefit the pediatric dental patient by reducing the time it takes for the analgesic effect as well as decreasing the pain during administration. Along with time, I will be using the Wong-Baker Scale to assess the pain. This scale is standard protocol for assessing pain in the pediatric population. The pediatric dental population has aversions to dental procedures because of the associated pain produced from most procedures. If limiting the time it takes for the analgesic to take effect and decrease the pain altogether, the pediatric patient will be less likely to skip treatment therefore, increase dental health.

Condition or Disease Intervention/Treatment Phase
  • Device: Onset Mixing Pen by Onpharma
  • Device: 2% lidocaine with 1:100,000 epinephrine
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
0 participants
Allocation:
Randomized
Intervention Model:
Single Group Assignment
Masking:
Double (Participant, Investigator)
Primary Purpose:
Treatment
Official Title:
The Efficacy of Analgesic Buffering With Sodium Bicarbonate for the Pediatric Dental Patient
Study Start Date :
Aug 1, 2013
Anticipated Primary Completion Date :
Feb 1, 2016
Anticipated Study Completion Date :
Feb 1, 2016

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: 2% lidocaine with 1:100,000 epinephrine

2% lidocaine with 1:100,000 epinephrine

Device: 2% lidocaine with 1:100,000 epinephrine
2% lidocaine with 1:100,000 epinephrine administered with a syringe prior to the procedure

Experimental: Onset Mixing Pen by Onpharma

Sodium Bicarbonate 8.4% mixed with the onset mixing pen

Device: Onset Mixing Pen by Onpharma
Sodium Bicarbonate 8.4%

Outcome Measures

Primary Outcome Measures

  1. Change in pain rating using the Wong-Baker scale [During injection (about 5 minutes)]

    By buffering the lidocaine/epinephrine injection, one should see a decrease in in pain during the administration of the anesthetic.

  2. Time it takes for buffered injection to take effect measured in minutes. [5 minutes]

    minutes for the analgesic effect to take place.

Eligibility Criteria

Criteria

Ages Eligible for Study:
5 Years to 12 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Current patients of Children's Hospital Colorado Dental Clinic

  • Existence of carious primary molars necessitating administration of an anesthetic agent

  • No history of post traumatic stress disorder or specific phobia related to a dental setting

  • No allergic reaction to lidocaine

  • Patient's between the ages of 5 to 12.

Exclusion Criteria:
  • Allergies to local anesthetics or sulfites

  • History of significant medical conditions

  • Taking any medications that may affect anesthetic assessment

  • Active sites of pathology in areas if injection

  • Outside the age range of 5 -12.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Children's Hospital Colorado Dental Clinic Aurora Colorado United States 80045

Sponsors and Collaborators

  • University of Colorado, Denver

Investigators

  • Principal Investigator: Valerie Esker, DMD, Children's Hospital Colorado Dental Clinic

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
University of Colorado, Denver
ClinicalTrials.gov Identifier:
NCT01883232
Other Study ID Numbers:
  • 13-0298
First Posted:
Jun 21, 2013
Last Update Posted:
Dec 17, 2015
Last Verified:
Dec 1, 2015
Additional relevant MeSH terms:

Study Results

No Results Posted as of Dec 17, 2015