The Efficacy of Analgesic Buffering With Sodium Bicarbonate for the Pediatric Dental Patient
1 other identifier
interventional
N/A
1 country
1
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
Started Aug 2013
Typical duration for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
May 17, 2013
CompletedFirst Posted
Study publicly available on registry
June 21, 2013
CompletedStudy Start
First participant enrolled
August 1, 2013
CompletedPrimary Completion
Last participant's last visit for primary outcome
February 1, 2016
CompletedStudy Completion
Last participant's last visit for all outcomes
February 1, 2016
CompletedDecember 17, 2015
December 1, 2015
2.5 years
May 17, 2013
December 16, 2015
Conditions
Outcome Measures
Primary Outcomes (2)
Change in pain rating using the Wong-Baker scale
By buffering the lidocaine/epinephrine injection, one should see a decrease in in pain during the administration of the anesthetic.
During injection (about 5 minutes)
Time it takes for buffered injection to take effect measured in minutes.
minutes for the analgesic effect to take place.
5 minutes
Study Arms (2)
2% lidocaine with 1:100,000 epinephrine
ACTIVE COMPARATOR2% lidocaine with 1:100,000 epinephrine
Onset Mixing Pen by Onpharma
EXPERIMENTALSodium Bicarbonate 8.4% mixed with the onset mixing pen
Interventions
2% lidocaine with 1:100,000 epinephrine administered with a syringe prior to the procedure
Eligibility Criteria
You may qualify if:
- 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.
You may not qualify if:
- 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.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Children's Hospital Colorado Dental Clinic
Aurora, Colorado, 80045, United States
Related Publications (9)
Kashyap VM, Desai R, Reddy PB, Menon S. Effect of alkalinisation of lignocaine for intraoral nerve block on pain during injection, and speed of onset of anaesthesia. Br J Oral Maxillofac Surg. 2011 Dec;49(8):e72-5. doi: 10.1016/j.bjoms.2011.04.068. Epub 2011 May 18.
PMID: 21592633RESULTGrassick P. The fear behind the fear: a case study of apparent simple injection phobia. J Behav Ther Exp Psychiatry. 1990 Dec;21(4):281-7. doi: 10.1016/0005-7916(90)90030-o.
PMID: 1982735RESULTArndt KA, Burton C, Noe JM. Minimizing the pain of local anesthesia. Plast Reconstr Surg. 1983 Nov;72(5):676-9. doi: 10.1097/00006534-198311000-00017.
PMID: 6622575RESULTMeit SS, Yasek V, Shannon CK, Hickman D, Williams D. Techniques for reducing anesthetic injection pain: an interdisciplinary survey of knowledge and application. J Am Dent Assoc. 2004 Sep;135(9):1243-50. doi: 10.14219/jada.archive.2004.0399.
PMID: 15493388RESULTBurns CA, Ferris G, Feng C, Cooper JZ, Brown MD. Decreasing the pain of local anesthesia: a prospective, double-blind comparison of buffered, premixed 1% lidocaine with epinephrine versus 1% lidocaine freshly mixed with epinephrine. J Am Acad Dermatol. 2006 Jan;54(1):128-31. doi: 10.1016/j.jaad.2005.06.043.
PMID: 16384767RESULTReed KL, Malamed SF, Fonner AM. Local anesthesia part 2: technical considerations. Anesth Prog. 2012 Fall;59(3):127-36; quiz 137. doi: 10.2344/0003-3006-59.3.127.
PMID: 23050753RESULTMalamed SF, Falkel M. Advances in local anesthetics: pH buffering and dissolved CO2. Dent Today. 2012 May;31(5):88-93; quiz 94-5. No abstract available.
PMID: 22650087RESULTChristoph RA, Buchanan L, Begalla K, Schwartz S. Pain reduction in local anesthetic administration through pH buffering. Ann Emerg Med. 1988 Feb;17(2):117-20. doi: 10.1016/s0196-0644(88)80293-2.
PMID: 2827545RESULTAminabadi NA, Farahani RM, Balayi Gajan E. The efficacy of distraction and counterstimulation in the reduction of pain reaction to intraoral injection by pediatric patients. J Contemp Dent Pract. 2008 Sep 1;9(6):33-40.
PMID: 18784857RESULT
Study Officials
- PRINCIPAL INVESTIGATOR
Valerie Esker, DMD
Children's Hospital Colorado Dental Clinic
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- DOUBLE
- Who Masked
- PARTICIPANT, INVESTIGATOR
- Purpose
- TREATMENT
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
May 17, 2013
First Posted
June 21, 2013
Study Start
August 1, 2013
Primary Completion
February 1, 2016
Study Completion
February 1, 2016
Last Updated
December 17, 2015
Record last verified: 2015-12