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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05378984
Other study ID # CHIMPS
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date March 1, 2020
Est. completion date December 20, 2020

Study information

Verified date May 2022
Source Karolinska Institutet
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This experimental randomized, double-blind, and controlled study included fifteen young, healthy, and pain-free men and 15 age-matched women. It lasted for three visits with at least one-week washout. Pain was experimentally induced, twice at each visit, with intramuscular injections of 0.2 mL hypertonic saline (5%), before and after intake of one of the different chocolate-types; white (30% cocoa-content), milk (34% cocoa-content), dark (70% cocoa-content). Pain duration, pain area, peak pain, and pressure pain threshold were assessed every fifth minute after each injection, between the time-points 5 to 30 min. Prior to inclusion, all participants underwent an examination in a dental chair. This included a clinical examination of the orofacial region according to the Diagnostic Criteria for temporomandibular disorders (DC/TMD) by a blinded examiner. Participants were also examined regarding their psychosocial status prior to inclusion, this included depression, somatization, anxiety, pain catastrophizing and stress.


Recruitment information / eligibility

Status Completed
Enrollment 30
Est. completion date December 20, 2020
Est. primary completion date December 20, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 40 Years
Eligibility Inclusion Criteria: 1. good general health 2. age between 18-40 years Exclusion Criteria: 1. any pain-related diagnosis of TMD or of the orofacial region 2. any headaches 3. a diagnosis of systemic muscular or joint diseases (fibromyalgia or rheumatoid arthritis) 4. whiplash-associated disorders 5. neurological disorders 6. psychiatric disorders 7. any allergy to the substances used

Study Design


Related Conditions & MeSH terms


Intervention

Other:
before - hypertonic saline 5%
pain was induced by intramuscular injections of hypertonic saline (5%)
after - hypertonic saline 5%
pain was induced by intramuscular injections of hypertonic saline (5%)

Locations

Country Name City State
Sweden Karolinska Institutet, Department of Dental Medicine Huddinge

Sponsors (1)

Lead Sponsor Collaborator
Karolinska Institutet

Country where clinical trial is conducted

Sweden, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in pain intensity by intake of chocolate Pain intensity will be assssed using a 0-100 visual analoge scale (0-no pain; 100-worst pain ever experienced) 5 min after injection of hypertonic saline
Primary Change in peak pain intensity before and after intake of chocolate Peak pain intensity will be asessed from the 0-100 visual analoge scale (0-no pain; 100-worst pain ever experienced) 5 min after injection of hypertonic saline
Primary Change in pain duration by intake of chocolate Pain duration is assessed in seconds. Pain duration up to 300 seconds after injection of hypertonic saline
Primary Change in pain area by intake of chocolate Pain area will be marked on lateral charts of the head before and after intake of chocolate and measured in au. Pain area is marked 5 min after injection of hypertonic saline
Secondary Change in pressure pain threshold by intake of chocolate Pressure pain thresholds are assessed using a digital algometer over the area of injection in the masseter muscle with a pressure rate of 30kPa/s. Pressure pain thresholds are assessed 5 min after injection of hypertonic saline
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