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Use of Acupuncture for Dental Pain: Testing a Model
This study has been completed.
First Received: February 2, 2001   Last Updated: August 17, 2006   History of Changes
Sponsor: National Center for Complementary and Alternative Medicine (NCCAM)
Collaborator: National Institute of Dental and Craniofacial Research (NIDCR)
Information provided by: National Center for Complementary and Alternative Medicine (NCCAM)
ClinicalTrials.gov Identifier: NCT00010972
  Purpose

This study is testing the safety and effectiveness of acupuncture in controlling pain related to the removal of partially impacted mandibular third molars. Acupuncture is the Chinese art of healing by inserting needles into the skin.

Participants ages 18 - 40 are given an initial x-ray to determine if one lower molar is partially bony impacted. Eligible participants will then undergo standard oral surgery to remove the impacted molar. A local anesthetic will be used prior to surgery. Directly after surgery the participant will be assigned to one of three groups. Participants will not be able to select which group they are assigned. Participants will receive either real or sham (fake) acupuncture as a treatment for post-extraction pain. After the initial acupuncture treatment, participants are required to remain for six hours at the dental site to be monitored. If a participants discomfort is measured as moderate or higher then a second acupuncture treatment will be administered. All participants will be administered questionnaires during the day of surgery. Participants will also be required to complete two diaries during the seven days following surgery. On the seventh day, participants return to have stitches removed and hand in completed diaries.


Condition Intervention Phase
Tooth, Impacted
Procedure: Acupuncture
Phase III

Study Type: Interventional
Study Design: Treatment, Randomized
Official Title: Use of Acupuncture for Dental Pain: Testing a Model

Resource links provided by NLM:

  Eligibility

Ages Eligible for Study:   18 Years to 40 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • At least one lower mandibular molar with partial bony impaction
  • General good health
  • Minimum body weight of 99 lbs.
  • Able to read and write in English
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00010972

Locations
United States, Maryland
Rivers Center Dental Associates
Columbia, Maryland, United States, 21046
Sponsors and Collaborators
Investigators
Principal Investigator: Sharon Nelson University of Maryland
  More Information

No publications provided

Study ID Numbers: R01 AT000010-01M, R01 AT000010-01
Study First Received: February 2, 2001
Last Updated: August 17, 2006
ClinicalTrials.gov Identifier: NCT00010972     History of Changes
Health Authority: United States: Federal Government

Additional relevant MeSH terms:
Tooth Diseases
Stomatognathic Diseases
Tooth, Impacted

ClinicalTrials.gov processed this record on November 09, 2009