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Clinical Trials/NCT00001597
NCT00001597
Completed
N/A

Pain Measurement in Healthy Volunteers

National Institute of Dental and Craniofacial Research (NIDCR)1 site in 1 country40 target enrollmentMarch 1997
ConditionsHealthyPain

Overview

Phase
N/A
Intervention
Not specified
Conditions
Healthy
Sponsor
National Institute of Dental and Craniofacial Research (NIDCR)
Enrollment
40
Locations
1
Status
Completed
Last Updated
18 years ago

Overview

Brief Summary

This study will attempt to develop and validate improved subjective measures of pain sensation and use these measures to evaluate pain sensitivity in patients.

Normal healthy volunteers and dental patients undergoing third molar extraction may be eligible for this study. Participants will undergo the following procedures:

Volunteers: Volunteers will participate in two 90-minute sessions in which they will receive and rate four heat stimuli per minute applied to the skin for a maximum of 36 minutes. The heat stimuli range from 37° (Degree)C to 51° (Degree)C (99° (Degree) F to 124° (Degree) F) and last 2 to 3 seconds. A drug commonly used in dental treatments may be administered during the second session. This will be either a maximum of 0.15 mg fentanyl, a short-acting narcotic pain killer, or a maximum of 5 mg saline, an inactive substance (placebo).

Dental patients: Dental patients will participate in two 60-minute sessions. The first session will be on the day before the third molar extraction, and the second session will be immediately before the dental procedure. The heat stimulus procedure will be identical to that described above for normal healthy volunteers.

Detailed Description

Mismanaged pain is still a major medical problem. Many pain syndromes have no effective treatment, and many are managed poorly. Basic and applied research on pain treatment is hampered by the unobservable nature of pain sensation and the lack of validated measures of this perception. The purpose of this protocol is to develop and validate improved subjective measures of pain sensation and use these measures to evaluate pain sensitivity in clinical populations. Normal volunteers rate experimentally-evoked pain sensations before and after double-blind administration of the opioid fentanyl or saline placebo. Patients rate experimentally-evoked pain sensations without any drug administration.

Registry
clinicaltrials.gov
Start Date
March 1997
End Date
June 2002
Last Updated
18 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
National Institute of Dental and Craniofacial Research (NIDCR)

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Not specified

Study Sites (1)

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