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Combined Medication for Improved Analgesia in Superficial Pain

Phase 3
Completed
Conditions
Pain
Interventions
Registration Number
NCT02194088
Lead Sponsor
Brigham and Women's Hospital
Brief Summary

This research study is being done to assess if a combination of medications can enhance the relief of superficial pain (pain at the surface of the skin, such as sunburn pain). The investigators also want to find out if certain genes may be linked to individual differences in experienced efficacy of pain killers. The combination of medications under investigation is diclofenac and atropine. Diclofenac has been approved by the U.S. Food and Drug Administration (FDA) to treat pain. Atropine has been approved by the FDA to treat certain types of poisoning, heartbeat problems, and other diseases but atropine is not approved to treat pain. However, atropine has been used for many years in different European countries to treat painful conditions such as stomach cramps.This research study will compare diclofenac and atropine to placebo.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
100
Inclusion Criteria
  • Male and female healthy volunteers.
  • 18-40 years of age.
  • Ability to read and understand English; English can be a second language provided that the participant feels that he/she understand all the questions used in the assessment measures.
Exclusion Criteria
  • Chronic pain condition or chronic or current treatment with any pain medication.
  • Presence of any illness or medication use that is judged to interfere with the trial. For example: psychiatric disorder, medication that can influence cognition or emotional processing, i.e. sleep medication, antidepressants, anti-convulsants or opioids.
  • Unwillingness to receive brief pain stimulation administered by a heat probe on the hand.
  • Allergy or contra-indication to receiving nonsteroidal anti-inflammatory medication and atropine (Treatment with antidepressants, neuroleptics, antihistaminic, levodopa, anti-acids. Pregnancy, breast-feeding, myasthenia gravis, pyloric stenosis, gastro-esophageal reflux, gastric ulcer, constipation, prostatic enlargement, glaucoma, cardio-pulmonary condition -including tachycardia, arrhythmia, arteriosclerosis-, hyperthyroidism, high blood pressure, genetic disease, kidney failure)

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
placeboPlaceboPlacebo capsules will be delivered in same number as the medication
Pain medication: diclofenac and atropineDiclofenac and Atropine combination drugDiclofenac and Atropine combination drug Provided PO. This is a novel combination. Diclofenac 100mg + Atropine 1.2 mg in one single dose
Primary Outcome Measures
NameTimeMethod
Pain Scores on Standardized Experimental Pain Testingbaseline and 1 hour pain measurement

Pain scores on standardized experimental pain testing, with collection of Visual analog scales (VAS) on a 0-100 scale 0 (no pain)- 100 (worst pain imaginable) Higher values represent a worse outcome (more pain)

Secondary Outcome Measures
NameTimeMethod
Catechol-O-methyltransferase (COMT) Polymorphism Correlation With Pain Reliefbaseline and 1 hour pain measurement

Difference in the baseline pain measurements compared to the 1-hour outcome measure will be correlated with Catechol-O-methyltransferase polymorphism

Side Effectsbaseline and 1 hour pain measurement

The investigators aimed assess if these would be a reason for discontinuation of treatment in a population with mild to moderate pain.Side effects will be assessed with a dichotomous measurement (yes/no)

Trial Locations

Locations (1)

Brigham And Women's Hospital

🇺🇸

Boston, Massachusetts, United States

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