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Sponsored by: |
Hadassah Medical Organization |
Information provided by: | Hadassah Medical Organization |
ClinicalTrials.gov Identifier: | NCT00363207 |
In children, behavior management is critical to the success of pediatric dental procedures. Most of the studies on local anesthesia performed in children deal with the question how to avoid or minimize pain during injection. Due to the sensation of numbness children scratch the soft tissues and bite lips and tongue. In many cases, this may be kept in children's memory as a "painful experience" and may affect their behavior in the following visit. The purpose of this study is to evaluate children's reactions to the administration of local anesthetic injection in the mandible (mandibular block) and in the maxilla (supraperiosteal infiltration), and to assess their behavior in the following visit related to each type of injection.
Condition |
Anesthesia, Local Anesthesia, Dental |
MedlinePlus related topics: | Anesthesia |
Study Type: | Observational |
Study Design: | Case-Crossover, Prospective |
Official Title: | Behavior of Children in the Following Appointment Related to Numbness Perception After Dental Local Anesthesia |
Estimated Enrollment: | 100 |
Study Start Date: | May 2007 |
Study Completion Date: | May 2008 |
Children between the ages of 4 to 7, undergoing dental treatment at the Department of Pediatric dentistry of the Hadassah School of Dental Medicine will participate in the study. All patients should be ASA Class I with no prior dental treatment who need at least two clinical sessions of similar operative procedures preceded by local anesthetic injection, one in each jaw, none of which due to emergency. Subjective and objective evaluation will be performed according to previously validated scales.
Ages Eligible for Study: | 4 Years to 8 Years |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | Yes |
Sampling Method: | Non-Probability Sample |
children receiving routine dental treatment at the hadassah school of dental medicine
Inclusion Criteria:
Exclusion Criteria:
Israel | |||||
Hadassah Medical Organization | |||||
Jerusalem, Israel, 91120 | |||||
Hadassah School of Dental Medicine | |||||
jerusalem, Israel, 91120 |
Hadassah Medical Organization |
Principal Investigator: | Diana Ram, Dr | Hadassah Medical Organization |
Responsible Party: | Hadassah Medical Organization ( Diana Ram ) |
Study ID Numbers: | STDI-HMO-CTIL |
First Received: | August 10, 2006 |
Last Updated: | May 19, 2008 |
ClinicalTrials.gov Identifier: | NCT00363207 |
Health Authority: | Israel: Israeli Health Ministry Pharmaceutical Administration |
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