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Pain and Placebo Analgesia. Does Extended Information About Dental Procedures Reduce Pain Induced by Dental Treatment?

Not Applicable
Completed
Conditions
Anxiety
Odontophobia
Interventions
Other: anesthetics and extended information before dental treatment
Other: anesthetics and standard information before dental treatment
Registration Number
NCT02160028
Lead Sponsor
Norwegian University of Science and Technology
Brief Summary

Information about the effectiveness of treatment has been found to reduce pain, termed placebo analgesia. In this study it will be investigated whether this finding translates to the dental clinic. It will be investigated whether information that suggested that minimal pain will be experienced during filling therapy, can reduce the pain associated with that procedure compared to a group that receives standard information. All patients will receive the same amount of anesthesia and similar procedures during filling therapy. It is predicted that extended information should reduce pain, and that the reduction in pain should be associated with a reduction in stress.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
52
Inclusion Criteria
  • Patients to be treated for dental caries
  • Patients should be able to read and communicate in Norwegian
Exclusion Criteria
  • Patients with life threatening diseases
  • Patients taking pain killers for other reasons on the day of treatment

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Extended informationanesthetics and extended information before dental treatmentThis group is given anesthetics and extended information before dental treatment about the anesthetics.
Standard informationanesthetics and standard information before dental treatmentThis group is given anesthetics and standard information before dental treatment about the anesthetics.
Primary Outcome Measures
NameTimeMethod
Reduction of pain1 hour

Pain intensity and pain discomfort will be measured by a VAS (Visual Analog Scale). The patients will report their experience of these factors verbally, four times during the treatment session.

Secondary Outcome Measures
NameTimeMethod
Reduction of stressOne hour

Stress is also measured using the VAS, i.e. using the same method as for pain. Stress or sympathetic activation is measured by using scin conductance on fingers (V-Amp (Brain Products, Munich, Germany).

Trial Locations

Locations (1)

Tannlegesenteret Madlagården, TSMG

🇳🇴

Hafrsfjord, Norway

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