Pain
Conditions
Keywords
Acupuncture, caffeine, pain
Brief summary
This is a single center, double blind, randomized, parallel-group study to assess the effect of 200mg caffeine,400mg caffeine and decaffeinated on acupuncture analgesia with the human pain model.
Detailed description
Aim: To evaluate the effect of caffeine on acupuncture analgesia with the human pain model. Design: Double blind, randomized controlled trial will be performed in Chengdu. The study including two pain models : Potassium pain model and Capsaicin pain model. Both models including the following several groups: 200mg caffeine group, 400mg caffeine group, and decaffeinated group. Participants will be randomly assign to the three groups. Each participants will receive coffee drinking and acupuncture intervention. Each subjects of the Potassium pain model will receive be measured the pain at baseline, 30 minutes after drinking coffee, 10, 20, 30 minutes during acupuncture and 30 minutes after acupuncture intervention completed. Blood samples will be collected at baseline, 30 minutes after drinking coffee, 30 minutes during acupuncture and 30 minutes after acupuncture intervention completed. Each subjects of the capsaicin pain model will be measured the spontaneous pain with VAS scale and the area of hyperalgesia with Von Frey hair at the time of 5 minutes after topical application of capsaicin , 30 minutes after drinking coffee, 10, 20, 30 minutes during acupuncture and 30 minutes after acupuncture intervention completed. Blood samples will be collected at the time of 5 minutes after topical application of capsaicin, 30 minutes after drinking coffee, 30 minutes during acupuncture and 30 minutes after acupuncture intervention completed.
Interventions
DEVICEacupuncture
therapeutic acupuncture treatment with actual needles
DIETARY_SUPPLEMENT200mg caffeine
8g coffee, po
DIETARY_SUPPLEMENT400mg caffeine
16g coffee, po
DIETARY_SUPPLEMENTDecaffeinated
decaffeinated coffee, po
Sponsors
University of Leipzig
Boston University
Chengdu University of Traditional Chinese Medicine
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)
Eligibility
Sex/Gender
ALL
Age
18 Years to 40 Years
Healthy volunteers
Yes
Inclusion criteria
* Age of a subject is between 18 and 40 years old, male or female * No known active ongoing disease, in good general health, with a BMI ranging from 18 to 30 kg/m2 * No history of mental disorders,infectious diseases and bleeding disorders. No history of allergic reaction. Females who are not pregnant, lactating, of child-bearing potential, or have no a pregnancy plan within 3 months * No smoking, drinking alcohol * No intake of beverage, food and alcohol ,which contains caffeine at least two hours * No use of any of the methyl purine drugs. No use of any of the drugs ,which can affect the half-life of caffeine, such as: cimetidine, steroids, growth hormone, etc * No previous experience with acupuncture or other related treatments within 3 days * Reliable, cooperative, and of adequate intelligence to record the requested information on the questionnaire form * Informed consent form must be signed by subjects
Exclusion criteria
* Subject with serious blood, heart, liver, kidney disease, digestive, or hematopoietic system disease * Subject with serious mental disorders, infectious diseases and bleeding disorders. Subject has a history of allergic reaction. Females who are pregnant, lactating, of child-bearing potential, or have a pregnancy plan within 3 months; * Prior use of any type of analgesic drugs before study within 5 half-lives of the drugs * Use of any of the methyl purine drugs. Use of any of the drugs, which can affect the half-life of caffeine, such as: Sympathomimetic drugs, theophylline drugs , α or β-blockers drugs, and any antihypertensive drugs, etc * Ingestion of any caffeine-containing beverage, food or alcohol 6 hours or less before study * Subject has a previous experience with acupuncture or other related treatments within 7 days * Suffered from medical or psychiatric disorders that prevented them from participating in the study * Subject who belongs to acupuncture-phobia
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Change of pain threshold will be measured with Potassium Pain Tester for potassium pain | Baseline, 30 minutes after drinking coffee,10,20,30 minutes during acupuncture and 30 minutes after acupuncture intervention completed |
| Change of pain will be measured with Visual Analog Scale for capsaicin pain | 5 minutes after topical application of capsaicin , 30 minutes after drinking coffee, 10, 20, 30 minutes during acupuncture and 30 minutes after acupuncture intervention completed. |
| Change of pain will be measured with Von Frey Hair for capsaicin pain | 5 minutes after topical application of capsaicin , 30 minutes after drinking coffee, 10, 20, 30 minutes during acupuncture and 30 minutes after acupuncture intervention completed. |
Secondary
| Measure | Time frame |
|---|---|
| The concentration of caffeine in plasma measured by high performance liquid chromatography in both models | one day after the study( blood samples were collected at Baseline, 30 minutes after drinking coffee,30 minutes during acupuncture and 30 minutes after acupuncture intervention completed. |
| The concentration of adenosine in plasma measured by high performance liquid | one day after the study( blood samples were collected at Baseline, 30 minutes after drinking coffee,30 minutes during acupuncture and 30 minutes after acupuncture intervention completed. |
Countries
China
Outcome results
None listed