Mechanisms of Acupuncture Analgesia on Experimental Dental Pain - A Psychophysical Study (Phase1) (MAC-DENT1)
Primary Purpose
Experimental Dental Pain
Status
Completed
Phase
Not Applicable
Locations
Switzerland
Study Type
Interventional
Intervention
Acupuncture
Sham-Acupuncture
No Acupuncture
Sponsored by
About this trial
This is an interventional treatment trial for Experimental Dental Pain focused on measuring Manual acupuncture, Experimental dental pain, Psychophysics, Autonomic nervous system, Subjective pain ratings
Eligibility Criteria
Inclusion Criteria:
- right-handed
- Written informed consent
- Fluent in German language
- Sufficient dental sensitivity for the tooth stimulation
- No acupuncture treatment in the previous 12 months
- No medical knowledge about acupuncure
Exclusion Criteria:
- Alcohol, drug, and analgesics consumption within the last 24 hours
- Complaints of diseases of the oral cavity
- Pre-existing neurological and(or psychiatric conditions
- History of severe dental pain
- Regular intake of pain medication
- History of brain injuries
- Alcohol and drug abuse
- Chronic diseases that require a permanent intake of drugs
Sites / Locations
- Clinic of Masticatory Disorders, Removable Prosthodontics, Geriatric and Special Care Dentistry Center of Dental Medicine University of Zurich
- Institute for Complementary and Integrative Medicine, University Hospital Zurich
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Healthy subjects
Arm Description
All subjects participate at 3 experimental conditions (Acupuncture, Sham-Acupuncture and No Acupuncture) at 3 different days in a randomized order.
Outcomes
Primary Outcome Measures
Comparison of the - mean post-pre acupuncture intervention pain intensity rating differences - and mean post-pre control intervention (no acupuncture) rating differences
Comparison of the - mean post-pre acupuncture intervention pain intensity rating differences - and mean post-pre sham-acupuncture rating differences
In case of a significant effect in outcome 1, outcome 2 will be tested using a hierarchical procedure in order to avoid multiple testing.
Secondary Outcome Measures
Longer lasting effects of acupuncture on subjective intensity ratings
Besides the pre-post intervention comparisons (primary outcome), 2 additional timepoints (Total: pre-intervention, post-intervention, 15 min post-intervention, 30 min post-intervention) will be examined to test differences in temporal dynamics between the 3 intervention effects on subjective pain intensity.
Longer lasting effects of acupuncture on pain-specific changes in heart rate.
Besides the pre-post intervention comparisons (primary outcome), 2 additional timepoints (Total: pre-intervention, post-intervention, 15 min post-intervention, 30 min post-intervention) will be examined to test differences in temporal dynamics between the 3 intervention effects on pain-specific heart rate alterations.
Longer lasting effects of acupuncture on pain-specific changes in skin conductance.
Besides the pre-post intervention comparisons (primary outcome), 2 additional timepoints (Total: pre-intervention, post-intervention, 15 min post-intervention, 30 min post-intervention) will be examined to test differences in temporal dynamics between the 3 intervention effects on pain-specific skin conductance alterations.
Longer lasting effects of acupuncture on pain-specific changes in respiratory frequency.
Besides the pre-post intervention comparisons (primary outcome), 2 additional timepoints (Total: pre-intervention, post-intervention, 15 min post-intervention, 30 min post-intervention) will be examined to test differences in temporal dynamics between the 3 intervention effects on pain-specific changes in respiratory frequency.
Changes in skin conductance during the three intervention types (acupuncture, sham-Acupuncture, no acupuncture).
Comparison of changes in the skin conductance measured during the acupuncture/sham-acupuncture and no acupuncture
Changes in heart rate variability (HRV) during the three intervention types (acupuncture, sham-Acupuncture, no acupuncture).
Comparison of changes in the HRV measured during the acupuncture/sham-acupuncture and no acupuncture
Changes in respiratory frequency during the three intervention types (acupuncture, sham-Acupuncture, no acupuncture).
Comparison of changes in respiratory frequency measured during the acupuncture/sham-acupuncture and no acupuncture.
Frequency of SAEs
Serious adverse event (SAEs) occurrences will be recorded and their frequency will be calculated.
Full Information
NCT ID
NCT02589418
First Posted
October 23, 2015
Last Updated
March 14, 2016
Sponsor
University of Zurich
Collaborators
First Teaching Hospital of Tianjin University of Traditional Chinese Medicine, Charite University, Berlin, Germany
1. Study Identification
Unique Protocol Identification Number
NCT02589418
Brief Title
Mechanisms of Acupuncture Analgesia on Experimental Dental Pain - A Psychophysical Study (Phase1)
Acronym
MAC-DENT1
Official Title
Mechanisms of Acupuncture Analgesia on Experimental Dental Pain - A Randomized, Single Blinded, Sham-controlled Psychophysical Study (Phase1)
Study Type
Interventional
2. Study Status
Record Verification Date
March 2016
Overall Recruitment Status
Completed
Study Start Date
October 2015 (undefined)
Primary Completion Date
March 2016 (Actual)
Study Completion Date
March 2016 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Zurich
Collaborators
First Teaching Hospital of Tianjin University of Traditional Chinese Medicine, Charite University, Berlin, Germany
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The investigators will assess the effects of manual acupuncture on experimental dental pain in 36 healthy subjects by means of subjective pain intensity ratings and pain-specific autonomic nervous system (ANS) reactions.
Detailed Description
This psychophysical and -physiological study is the first part of a two-phase project which pursues to explore how acupuncture-induced pain modulation interacts with pain-specific brain processing patterns by means of functional magnetic resonance imaging (fMRI) and by using an experimental dental pain model.
In this preceding study, the characterization of manual acupuncture effects on the experimental dental pain model will be tested under laboratory conditions and without restrictions of an fMRI-measurement in order to provide a sound foundation for the following fMRI-experiment. Pain modulating effects of the manual acupuncture intervention (4 points: needle manipulation of bilateral large-intestine 4 (LI4), stomach 6 and 7 (ST6, ST7) ipsilateral to the stimulated tooth) will be compared to sham-acupuncture (insertion and manipulation of 4 non-acupuncture points) and a control intervention (no acupuncture) which will each be performed at 3 different days in a randomized order. Intervention effects on experimental dental pain will be assessed by testing of 36 healthy volunteers by means of subjective pain intensity ratings and pain-specific ANS reactions such as electrodermal activity and heart rate/respiratory changes. Besides laying the groundwork for the following fMRI experiment, this study could provide valuable basic insights into the dynamics of the tested manual acupuncture effects and further provide important knowledge for the planning of future clinical studies encompassing dental conditions and development of acupuncture treatments.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Experimental Dental Pain
Keywords
Manual acupuncture, Experimental dental pain, Psychophysics, Autonomic nervous system, Subjective pain ratings
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
Participant
Allocation
N/A
Enrollment
35 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Healthy subjects
Arm Type
Experimental
Arm Description
All subjects participate at 3 experimental conditions (Acupuncture, Sham-Acupuncture and No Acupuncture) at 3 different days in a randomized order.
Intervention Type
Procedure
Intervention Name(s)
Acupuncture
Other Intervention Name(s)
Verum Acupuncture
Intervention Description
Needle insertion and manipulation at 4 acupuncture points (bilateral LI4, right ST6 and ST7).
Intervention Type
Procedure
Intervention Name(s)
Sham-Acupuncture
Intervention Description
Needle insertion and manipulation at 4 non-acupoints
Intervention Type
Procedure
Intervention Name(s)
No Acupuncture
Intervention Description
Control intervention: No needle insertion and manipulation
Primary Outcome Measure Information:
Title
Comparison of the - mean post-pre acupuncture intervention pain intensity rating differences - and mean post-pre control intervention (no acupuncture) rating differences
Time Frame
15 minutes
Title
Comparison of the - mean post-pre acupuncture intervention pain intensity rating differences - and mean post-pre sham-acupuncture rating differences
Description
In case of a significant effect in outcome 1, outcome 2 will be tested using a hierarchical procedure in order to avoid multiple testing.
Time Frame
15 minutes
Secondary Outcome Measure Information:
Title
Longer lasting effects of acupuncture on subjective intensity ratings
Description
Besides the pre-post intervention comparisons (primary outcome), 2 additional timepoints (Total: pre-intervention, post-intervention, 15 min post-intervention, 30 min post-intervention) will be examined to test differences in temporal dynamics between the 3 intervention effects on subjective pain intensity.
Time Frame
50 minutes
Title
Longer lasting effects of acupuncture on pain-specific changes in heart rate.
Description
Besides the pre-post intervention comparisons (primary outcome), 2 additional timepoints (Total: pre-intervention, post-intervention, 15 min post-intervention, 30 min post-intervention) will be examined to test differences in temporal dynamics between the 3 intervention effects on pain-specific heart rate alterations.
Time Frame
50 minutes
Title
Longer lasting effects of acupuncture on pain-specific changes in skin conductance.
Description
Besides the pre-post intervention comparisons (primary outcome), 2 additional timepoints (Total: pre-intervention, post-intervention, 15 min post-intervention, 30 min post-intervention) will be examined to test differences in temporal dynamics between the 3 intervention effects on pain-specific skin conductance alterations.
Time Frame
50 minutes
Title
Longer lasting effects of acupuncture on pain-specific changes in respiratory frequency.
Description
Besides the pre-post intervention comparisons (primary outcome), 2 additional timepoints (Total: pre-intervention, post-intervention, 15 min post-intervention, 30 min post-intervention) will be examined to test differences in temporal dynamics between the 3 intervention effects on pain-specific changes in respiratory frequency.
Time Frame
50 minutes
Title
Changes in skin conductance during the three intervention types (acupuncture, sham-Acupuncture, no acupuncture).
Description
Comparison of changes in the skin conductance measured during the acupuncture/sham-acupuncture and no acupuncture
Time Frame
10 minutes
Title
Changes in heart rate variability (HRV) during the three intervention types (acupuncture, sham-Acupuncture, no acupuncture).
Description
Comparison of changes in the HRV measured during the acupuncture/sham-acupuncture and no acupuncture
Time Frame
10 minutes
Title
Changes in respiratory frequency during the three intervention types (acupuncture, sham-Acupuncture, no acupuncture).
Description
Comparison of changes in respiratory frequency measured during the acupuncture/sham-acupuncture and no acupuncture.
Time Frame
10 minutes
Title
Frequency of SAEs
Description
Serious adverse event (SAEs) occurrences will be recorded and their frequency will be calculated.
Time Frame
1 month
Other Pre-specified Outcome Measures:
Title
Expectation towards acupuncture
Description
Acupuncture expectation will be assessed using an acupuncture expectation questionnaire developed by the Institut for Complementary and Integrative Medicine, University Hospital Zurich
Time Frame
60 minutes
Title
Anxiety states and traits
Description
For the assessment of anxiety levels, the State-Trait Anxiety Inventory(STAI)(Bieling et al., 1998) questionnaire will be applied.
Time Frame
60 minutes
10. Eligibility
Sex
Male
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
40 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
right-handed
Written informed consent
Fluent in German language
Sufficient dental sensitivity for the tooth stimulation
No acupuncture treatment in the previous 12 months
No medical knowledge about acupuncure
Exclusion Criteria:
Alcohol, drug, and analgesics consumption within the last 24 hours
Complaints of diseases of the oral cavity
Pre-existing neurological and(or psychiatric conditions
History of severe dental pain
Regular intake of pain medication
History of brain injuries
Alcohol and drug abuse
Chronic diseases that require a permanent intake of drugs
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Claudia M Witt, MD
Organizational Affiliation
University of Zurich
Official's Role
Principal Investigator
Facility Information:
Facility Name
Clinic of Masticatory Disorders, Removable Prosthodontics, Geriatric and Special Care Dentistry Center of Dental Medicine University of Zurich
City
Zurich
ZIP/Postal Code
8032
Country
Switzerland
Facility Name
Institute for Complementary and Integrative Medicine, University Hospital Zurich
City
Zurich
ZIP/Postal Code
8091
Country
Switzerland
12. IPD Sharing Statement
Citations:
PubMed Identifier
9682533
Citation
Bieling PJ, Antony MM, Swinson RP. The State-Trait Anxiety Inventory, Trait version: structure and content re-examined. Behav Res Ther. 1998 Jul-Aug;36(7-8):777-88. doi: 10.1016/s0005-7967(98)00023-0.
Results Reference
background
PubMed Identifier
31521794
Citation
de Matos NMP, Pach D, Xing JJ, Barth J, Beyer LE, Shi X, Kern A, Lukic N, Ettlin DA, Brugger M, Witt CM. Evaluating the Effects of Acupuncture Using a Dental Pain Model in Healthy Subjects - A Randomized, Cross-Over Trial. J Pain. 2020 Mar-Apr;21(3-4):440-454. doi: 10.1016/j.jpain.2019.08.013. Epub 2019 Sep 12.
Results Reference
derived
Learn more about this trial
Mechanisms of Acupuncture Analgesia on Experimental Dental Pain - A Psychophysical Study (Phase1)
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