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Efficacy of Co-administration of an NSAID With a Dopamine Agonist In Healthy Subjects

Primary Purpose

Acute Pain

Status
Withdrawn
Phase
Phase 2
Locations
Study Type
Interventional
Intervention
Naproxen
Sinemet
Sinemet
Placebo
Sponsored by
Northwestern University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Acute Pain focused on measuring acute, pain

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

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

    Arm Type

    Placebo Comparator

    Active Comparator

    Active Comparator

    Active Comparator

    Arm Label

    Control Group

    Standard Treatment / Positive Control Group

    Experimental Group #1

    Experimental Group #2

    Arm Description

    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 )

    Outcomes

    Primary Outcome Measures

    VAS pain scale

    Secondary Outcome Measures

    Full Information

    First Posted
    February 17, 2014
    Last Updated
    October 9, 2014
    Sponsor
    Northwestern University
    Collaborators
    National Institute of Dental and Craniofacial Research (NIDCR), National Institutes of Health (NIH)
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    1. Study Identification

    Unique Protocol Identification Number
    NCT02116790
    Brief Title
    Efficacy of Co-administration of an NSAID With a Dopamine Agonist In Healthy Subjects
    Official Title
    Study of the Efficacy of Co-administration of an NSAID With a Dopamine Agonist in the Alleviation of Acute Cutaneous Inflammatory Pain in Healthy Subjects
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    October 2014
    Overall Recruitment Status
    Withdrawn
    Study Start Date
    May 2014 (undefined)
    Primary Completion Date
    January 2015 (Anticipated)
    Study Completion Date
    January 2015 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Northwestern University
    Collaborators
    National Institute of Dental and Craniofacial Research (NIDCR), National Institutes of Health (NIH)

    4. Oversight

    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    Findings from the investigator's lab and others' show the involvement of the brain's mesolimbic circuitry in pain perception and evaluation, as well as during the transition from acute to chronic pain states in both humans and animals. Dopamine (DA) is one of the main neurotransmitters in this circuitry, and it is possible it could have an intimate role in pain processing, chronicity, and related anatomical and functional neuroplasticity. In this study, the investigators first need to know if the combination of l-dopa and Naproxen is safe and efficacious in humans with acute pain, and if so, at what doses. For the present study, healthy pain-free participants will be injected with a small bolus of capsaicin subcutaneously to induce acute cutaneous inflammatory pain. Capsaicin is ideal for this study because it causes a characteristic inflammatory response that is almost always accompanied with pain, has a well-validated dose-response curve, and has effects that will go away completely in a few hours after administration, causing no permanent damage to study subjects. Effects of capsaicin will be measured by changes (decreases) from baseline in thermal and tactile thresholds, as well as by verbally reported cutaneous pain levels (on a scale from 0-10). Participants will also be given study medication in the form of a placebo, one drug, or a combination of drugs before capsaicin injection to allow for any analgesic effects to peak before pain onset. For those receiving active medication, they will either receive Naproxen with placebo or the combination of naproxen and l-dopa (the latter of which will be in one of two different doses). This will allow the investigators to investigate (1) whether co-administration of naproxen and l-dopa has analgesic effects in low levels of acute pain in humans, (2) if this combination is pain-alleviating, whether it is equally as or more efficacious than naproxen, which is the clinical standard of treatment, and finally (3) what dose provides the most analgesia.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Acute Pain
    Keywords
    acute, pain

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Phase 2
    Interventional Study Model
    Parallel Assignment
    Masking
    ParticipantInvestigatorOutcomes Assessor
    Allocation
    Randomized
    Enrollment
    0 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    Control Group
    Arm Type
    Placebo Comparator
    Arm Description
    10 participants will be given two pills: both will be placebos
    Arm Title
    Standard Treatment / Positive Control Group
    Arm Type
    Active Comparator
    Arm Description
    10 participants will be given two pills: both will be Naproxen (each pill = 250mg, total dose = 500mg)
    Arm Title
    Experimental Group #1
    Arm Type
    Active Comparator
    Arm Description
    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)
    Arm Title
    Experimental Group #2
    Arm Type
    Active Comparator
    Arm Description
    10 participants will be given two pills: one will be Naproxen (250 mg) and the other will be of Sinemet (carbidopa/levodopa 25mg/100mg )
    Intervention Type
    Drug
    Intervention Name(s)
    Naproxen
    Other Intervention Name(s)
    Aleve, Anaprox, Antalgin, Apranax, Feminax Ultra, Flanax, Inza, Midol Extended Relief, Nalgesin, Naposin, Naprelan, Naprogesic, Naprosyn, Narocin, Proxen, Soproxen, Synflex, Xenobid
    Intervention Description
    Subjects will take one 250mg Naproxen capsule
    Intervention Type
    Drug
    Intervention Name(s)
    Sinemet
    Other Intervention Name(s)
    Carbidopa/levodopa, Levocarb, Pharmacopa, Atamet, Apo-Levocarb, Co-careldopa
    Intervention Description
    Subjects will take one 12.5mg/50mg Sinemet.
    Intervention Type
    Drug
    Intervention Name(s)
    Sinemet
    Other Intervention Name(s)
    Carbidopa/levodopa, Levocarb, Pharmacopa, Atamet, Apo-Levocarb, Co-careldopa
    Intervention Description
    Subjects will take one 25mg/100mg Sinemet.
    Intervention Type
    Drug
    Intervention Name(s)
    Placebo
    Other Intervention Name(s)
    Sugar Pill
    Intervention Description
    Subjects will take two placebos.
    Primary Outcome Measure Information:
    Title
    VAS pain scale
    Time Frame
    1 Day

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    Accepts Healthy Volunteers
    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
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Apkar V Apkarian, PhD
    Organizational Affiliation
    Northwestern University
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

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    Efficacy of Co-administration of an NSAID With a Dopamine Agonist In Healthy Subjects

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