Efficacy of Co-administration of an NSAID With a Dopamine Agonist In Healthy Subjects
Acute Pain
About this trial
This is an interventional treatment trial for Acute Pain focused on measuring acute, pain
Eligibility Criteria
Inclusion Criteria:
- Must be currently healthy and have none of the exclusion criteria listed below.
- Must be at least 18 years of age.
- Must be able to communicate (speak and write) in English.
- Must demonstrate that they understand what the study entails and requires of them.
- Must be able to dedicate the amount of time (~3 hours) to participate in the study.
Exclusion Criteria:
- History of chronic pain of any kind
- Have a current episode of acute pain of any kind (including stomach ache, headache, muscle ache, etc)
- History of psychiatric illness or brain injury
- History of substance abuse
- History of motor impairments
- History of another chronic disease (such as heart disease, celiac's, bronchial asthma, etc)
- Have a diagnosis of narrow-angle glaucoma
- History or presence of high blood pressure
- History or presence of melanoma cancer
- Currently on a high-protein diet
- Women who are pregnant, trying to get pregnant, or breastfeeding
- Known or suspected allergies to capsaicin, peppers, levodopa, carbidopa, naproxen, NSAIDs, rubbing alcohol (in the medical wipes), or lidocaine
- History or presence of dermatological disorder, including contact dermatitis and a history of skin allergies in general
- Presence of a skin lesion in the areas to be tested
Prohibited Medication:
- Aliskiren
- ACE inhibitors
- Angiotensin 2 receptor blockers
- Cidofovir
- Corticosteroids
- Anti-platelet drugs
- Blood-thinners
- Another NSAID
- MAOIs
- Tetrabenazine
- Anti-depressants
- Anti-psychotics
- Metoclopramide
- Phenytoin
- Papaverine
- Sedatives or muscle relaxers
- Tryptan/L-tryptophan
- DA agonists/antagonists
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
Placebo Comparator
Active Comparator
Active Comparator
Active Comparator
Control Group
Standard Treatment / Positive Control Group
Experimental Group #1
Experimental Group #2
10 participants will be given two pills: both will be placebos
10 participants will be given two pills: both will be Naproxen (each pill = 250mg, total dose = 500mg)
10 participants will be given two pills: one will be Naproxen (250 mg) and the other will be of Sinemet (carbidopa/levodopa 12.5mg/50mg)
10 participants will be given two pills: one will be Naproxen (250 mg) and the other will be of Sinemet (carbidopa/levodopa 25mg/100mg )