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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02160028
Other study ID # 2014/2615/SGK
Secondary ID
Status Completed
Phase N/A
First received June 6, 2014
Last updated February 12, 2017
Start date August 2014
Est. completion date January 2015

Study information

Verified date February 2017
Source Norwegian University of Science and Technology
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


Recruitment information / eligibility

Status Completed
Enrollment 52
Est. completion date January 2015
Est. primary completion date January 2015
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group N/A and older
Eligibility 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


Related Conditions & MeSH terms


Intervention

Other:
anesthetics and extended information before dental treatment
The extended information is a comprehensive explanation about what to expect of the treatment and the anesthetic method, phrased in positive words and opening up for questions after information is given.
anesthetics and standard information before dental treatment
The standard information is short and concise, telling in neutral words what to expect.

Locations

Country Name City State
Norway Tannlegesenteret Madlagården, TSMG Hafrsfjord

Sponsors (4)

Lead Sponsor Collaborator
Norwegian University of Science and Technology Tannhelsetjenestens Kompetansesenter Vest, TK Vest, Tannlegesenteret Madlagården, TSMG, University of Bergen

Country where clinical trial is conducted

Norway, 

Outcome

Type Measure Description Time frame Safety issue
Primary Reduction of pain 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. 1 hour
Secondary Reduction of stress 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). One hour
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