- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01986283
Abuse Potential Study of PF-00345439
March 31, 2016 updated by: Pain Therapeutics
A Randomized, Double-blind, Triple-dummy, Placebo Controlled, Single-dose, 4-way Crossover Study To Determine The Relative Abuse Potential Of Pf-00345439 (Oxycodone Extended Release Capsules) Compared To Immediate-release Oxycodone And Placebo When Administered Orally Whole And/or Chewed To Non-dependent, Recreational Opioid Users Under Fasted Conditions
This study will determine the relative abuse potential of intact and chewed PF-00345439 (Oxycodone Extended-Release Capsules) compared to crushed oxycodone HCL immediate release (IR) tablets and placebo administered orally to non-dependent, recreational opioid users.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
67
Phase
- Phase 1
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Utah
-
Salt Lake City, Utah, United States, 84106
- Lifetree Clinical Research
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 55 years (Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Healthy male and/or female subjects between the ages of 18 and 55 years who are recreational opioid users and are NOT dependent on opioids.
Exclusion Criteria:
- Evidence or history of clinically significant medical conditions.
- Diagnosis of substance and/or alcohol dependence (excluding caffeine and nicotine).
- Has participated in, is currently participating in, or is seeking treatment for substance-and/or alcohol-related disorders (excluding nicotine and caffeine).
- Has a positive urine drug screen (UDS) excluding tetrahydrocannabinol (THC).
- Has a positive alcohol breath test.
- Has any history of a condition in which an opioid is contraindicated.
- History of sleep apnea in the past 5 years that has not been resolved or corrected.
- Other severe acute or chronic medical or psychiatric condition or laboratory abnormality that may increase the risk associated with study participation or investigational product administration or may interfere with the interpretation of study results .
- Positive test for Hepatitis B, Hepatitis C, or HIV.
- Allergy or history of hypersensitivity to naloxone HCl, oxycodone HCl, other opioids, and/or lactose.
- Any condition possibly affecting drug absorption (eg, gastrectomy).
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Basic Science
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Placebo Comparator: Treatment A
Placebo solution +placebo capsule + placebo capsule chewed.
|
Taken once
|
|
Experimental: Treatment B
PF-00345439 taken whole + placebo solution + placebo chewed
|
40 mg capsule swallowed whole, taken once
40 mg capsule chewed, taken once
|
|
Experimental: Treatment C
PF-00345439 chewed + placebo solution + placebo taken whole
|
40 mg capsule swallowed whole, taken once
40 mg capsule chewed, taken once
|
|
Active Comparator: Treatment D
Oxycodone HCl immediate-release 40 mg tablets (eg, 2 x 5 mg + 1 x 30 mg) + placebo taken whole + placebo chewed
|
40 mg solution, taken once
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Drug Liking: Peak Effect (Emax)
Time Frame: 12 hours
|
Drug liking assesses the degree that a participant likes a drug effect at the time the question is being asked (that is, at the moment).
It is scored using a 100 mm unipolar visual analogue scale (VAS); where 0 mm = Not at all and 100 mm = Extremely.
|
12 hours
|
|
High: Peak Effect (Emax)
Time Frame: 12 hours
|
High assesses the degree that a subject feels a good effect (ie euphoria) at the time the question is being asked (that is, at the moment).
It is scored using a 100 mm unipolar scale); where 0 mm = Not at all and 100 mm = Extremely.
|
12 hours
|
|
Drug Liking: Area Under Effect Curve (AUE) From 0-2 Hours
Time Frame: 2 hours
|
Drug liking assesses the degree that a participant likes a drug effect at the time the question is being asked (that is, at the moment).
It is scored using a 100 mm unipolar visual analogue scale (VAS); where 0 mm = Not at all and 100 mm = Extremely.
|
2 hours
|
|
High: Area Under Effect Curve (AUE) From 0-2 Hours
Time Frame: 2 hours
|
High assesses the degree that a subject feels a good effect (ie euphoria) at the time the question is being asked (that is, at the moment).
It is scored using a 100 mm unipolar scale); where 0 mm = Not at all and 100 mm = Extremely.
|
2 hours
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Take Drug Again Effect at 24 Hours
Time Frame: 24 hours
|
Take drug again visual analogue scale (VAS) is a subjective assessment of the degree to which a participant would desire to take the drug again if given the opportunity.
It is presented on a 100 mm VAS with score ranging from 0 mm to 100 mm (score of 0 mm = Definately not and score of 100 mm = Definately so).
|
24 hours
|
|
Overall Drug Liking
Time Frame: 24 hours
|
Overall Drug Liking visual analogue scale (VAS) is a subjective assessment of the degree to which a participant likes the drug overall.
It is presented on a 100 mm VAS with score ranging from 0 mm to 100 mm (score of 0 mm = Not at all and 100 mm = Extremely).
|
24 hours
|
|
Any Drug Effects: Area Under Drug Effect Curve (AUE) From 0-1 Hour
Time Frame: 1 hour
|
Any drug effects effects VAS assesses the effect experienced by the participant on a 100 mm unipolar VAS, where responses are unidirectional and range from a response of 'not at all' (score of 0 mm) to 'extremely' (score of 100 mm).
AUE (0-1) = Area under the effect versus time curve from time zero to time of last quantifiable effect (0-1).
|
1 hour
|
|
Pupillometry: Area Under Effect Curve (AUE) From 0-1 Hour
Time Frame: 1 hour
|
Pupillometry assessments measured change in pupil size (miosis) as an indicator of opioid pharmacological properties.
The same eye for each participant was used for all measurements during the study.
Participants had the size of their pupil measured (in mm) using a pupillometer.
Measurements were made in a dimly lit (mesopic) room with controlled lighting conditions.
AUE (0-1) = Area under the effect versus time curve from time zero to time of last quantifiable effect (0-1).
|
1 hour
|
|
Chewing Duration
Time Frame: 5 min
|
Chewing duration is a measurement of the total time a person is able to chew.
|
5 min
|
|
Taste: Subjective Experience from Chewing
Time Frame: 5 min
|
Subjective Experience from Chewing is a visual analogue scale (VAS) subjective assessment of the taste of the substance being chewed.
Participants are asked to describe the taste of the drug using a VAS with score ranging from 0 mm to 100 mm (score of 0 mm = Extremely unpleasant, 50 mm = neutral, and 100 mm = Extremely pleasant).
|
5 min
|
|
Any Drug Effects: Area Under Drug Effect Curve (AUE) From 0-2 Hours
Time Frame: 2 hours
|
Any drug effects effects VAS assesses the effect experienced by the participant on a 100 mm unipolar VAS, where responses are unidirectional and range from a response of 'not at all' (score of 0 mm) to 'extremely' (score of 100 mm).
AUE (0-2) = Area under the effect versus time curve from time zero to time of last quantifiable effect (0-2).
|
2 hours
|
|
Any Drug Effects: Area Under Drug Effect Curve (AUE) From 0-3 Hours
Time Frame: 3 hours
|
Any drug effects effects VAS assesses the effect experienced by the participant on a 100 mm unipolar VAS, where responses are unidirectional and range from a response of 'not at all' (score of 0 mm) to 'extremely' (score of 100 mm).
AUE (0-3) = Area under the effect versus time curve from time zero to time of last quantifiable effect (0-3).
|
3 hours
|
|
Any Drug Effects: Area Under Drug Effect Curve (AUE) From 0-12 Hours
Time Frame: 12 hours
|
Any drug effects effects VAS assesses the effect experienced by the participant on a 100 mm unipolar VAS, where responses are unidirectional and range from a response of 'not at all' (score of 0 mm) to 'extremely' (score of 100 mm).
AUE (0-12) = Area under the effect versus time curve from time zero to time of last quantifiable effect (0-12).
|
12 hours
|
|
Pupillometry: Area Under Effect Curve (AUE) From 0-2 Hours
Time Frame: 2 hours
|
Pupillometry assessments measured change in pupil size (miosis) as an indicator of opioid pharmacological properties.
The same eye for each participant was used for all measurements during the study.
Participants had the size of their pupil measured (in mm) using a pupillometer.
Measurements were made in a dimly lit (mesopic) room with controlled lighting conditions.
AUE (0-2) = Area under the effect versus time curve from time zero to time of last quantifiable effect (0-2).
|
2 hours
|
|
Pupillometry: Area Under Effect Curve (AUE) From 0-3 Hours
Time Frame: 3 hours
|
Pupillometry assessments measured change in pupil size (miosis) as an indicator of opioid pharmacological properties.
The same eye for each participant was used for all measurements during the study.
Participants had the size of their pupil measured (in mm) using a pupillometer.
Measurements were made in a dimly lit (mesopic) room with controlled lighting conditions.
AUE (0-3) = Area under the effect versus time curve from time zero to time of last quantifiable effect (0-3).
|
3 hours
|
|
Pupillometry: Area Under Effect Curve (AUE) From 0-12 Hours
Time Frame: 12 hours
|
Pupillometry assessments measured change in pupil size (miosis) as an indicator of opioid pharmacological properties.
The same eye for each participant was used for all measurements during the study.
Participants had the size of their pupil measured (in mm) using a pupillometer.
Measurements were made in a dimly lit (mesopic) room with controlled lighting conditions.
AUE (0-12) = Area under the effect versus time curve from time zero to time of last quantifiable effect (0-12).
|
12 hours
|
|
High: Area Under Effect Curve (AUE) From 0-1 Hour
Time Frame: 1 hour
|
High VAS assesses the effect experienced by the participant on a 100 mm unipolar VAS, where responses are unidirectional and range from a response of 'not at all' (score of 0 mm) to 'extremely' (score of 100 mm).
AUE (0-1) = Area under the effect versus time curve from time zero to time of last quantifiable effect (0-1).
|
1 hour
|
|
High: Area Under Effect Curve (AUE) From 0-3 Hours
Time Frame: 3 hours
|
High VAS assesses the effect experienced by the participant on a 100 mm unipolar VAS, where responses are unidirectional and range from a response of 'not at all' (score of 0 mm) to 'extremely' (score of 100 mm).
AUE (0-3) = Area under the effect versus time curve from time zero to time of last quantifiable effect (0-3).
|
3 hours
|
|
High: Area Under Effect Curve (AUE) From 0-12 Hours
Time Frame: 12 hours
|
High VAS assesses the effect experienced by the participant on a 100 mm unipolar VAS, where responses are unidirectional and range from a response of 'not at all' (score of 0 mm) to 'extremely' (score of 100 mm).
AUE (0-12) = Area under the effect versus time curve from time zero to time of last quantifiable effect (0-12).
|
12 hours
|
|
Good Drug Effects: Area Under Drug Effect Curve (AUE) From 0-1 Hour
Time Frame: 1 hour
|
Good drug effects VAS assesses the effect experienced by the participant on a 100 mm unipolar VAS, where responses are unidirectional and range from a response of 'not at all' (score of 0 mm) to 'extremely' (score of 100 mm).
AUE (0-1) = Area under the effect versus time curve from time zero to time of last quantifiable effect (0-1).
|
1 hour
|
|
Good Drug Effects: Area Under Effect Curve (AUE) From 0-2 Hours
Time Frame: 2 hours
|
Good drug effects VAS assesses the effect experienced by the participant on a 100 mm unipolar VAS, where responses are unidirectional and range from a response of 'not at all' (score of 0 mm) to 'extremely' (score of 100 mm).
AUE (0-2) = Area under the effect versus time curve from time zero to time of last quantifiable effect (0-2).
|
2 hours
|
|
Good Drug Effects: Area Under Effect Curve (AUE) From 0-3 Hours
Time Frame: 3 hours
|
Good drug effects VAS assesses the effect experienced by the participant on a 100 mm unipolar VAS, where responses are unidirectional and range from a response of 'not at all' (score of 0 mm) to 'extremely' (score of 100 mm).
AUE (0-3) = Area under the effect versus time curve from time zero to time of last quantifiable effect (0-3).
|
3 hours
|
|
Good Drug Effects: Area Under Effect Curve (AUE) From 0-12 Hours
Time Frame: 12 hours
|
Good drug effects VAS assesses the effect experienced by the participant on a 100 mm unipolar VAS, where responses are unidirectional and range from a response of 'not at all' (score of 0 mm) to 'extremely' (score of 100 mm).
AUE (0-12) = Area under the effect versus time curve from time zero to time of last quantifiable effect (0-12).
|
12 hours
|
|
Bad Drug Effects: Area Under Effect Curve (AUE) From 0-1 Hour
Time Frame: 1 hour
|
Bad drug effects VAS assesses the effect experienced by the participant on a 100 mm unipolar VAS, where responses are unidirectional and range from a response of 'not at all' (score of 0 mm) to 'extremely' (score of 100 mm).
AUE (0-1) = Area under the effect versus time curve from time zero to time of last quantifiable effect (0-1).
|
1 hour
|
|
Bad Drug Effects: Area Under Effect Curve (AUE) From 0-2 Hours
Time Frame: 2 hour
|
Bad drug effects VAS assesses the effect experienced by the participant on a 100 mm unipolar VAS, where responses are unidirectional and range from a response of 'not at all' (score of 0 mm) to 'extremely' (score of 100 mm).
AUE (0-2) = Area under the effect versus time curve from time zero to time of last quantifiable effect (0-2).
|
2 hour
|
|
Bad Drug Effects: Area Under Effect Curve (AUE) From 0-3 Hours
Time Frame: 3 hours
|
Bad drug effects VAS assesses the effect experienced by the participant on a 100 mm unipolar VAS, where responses are unidirectional and range from a response of 'not at all' (score of 0 mm) to 'extremely' (score of 100 mm).
AUE (0-3) = Area under the effect versus time curve from time zero to time of last quantifiable effect (0-3).
|
3 hours
|
|
Bad Drug Effects: Area Under Effect Curve (AUE) From 0-12 Hours
Time Frame: 12 hours
|
Bad drug effects VAS assesses the effect experienced by the participant on a 100 mm unipolar VAS, where responses are unidirectional and range from a response of 'not at all' (score of 0 mm) to 'extremely' (score of 100 mm).
AUE (0-12) = Area under the effect versus time curve from time zero to time of last quantifiable effect (0-12).
|
12 hours
|
|
Feeling Sick: Area Under Effect Curve (AUE) From 0-1 Hour
Time Frame: 1 hour
|
Feeling sick VAS assesses the effect experienced by the participant on a 100 mm unipolar VAS, where responses are unidirectional and range from a response of 'not at all' (score of 0 mm) to 'extremely' (score of 100 mm).
AUE (0-1) = Area under the effect versus time curve from time zero to time of last quantifiable effect (0-1).
|
1 hour
|
|
Feeling Sick: Area Under Effect Curve (AUE) From 0-2 Hours
Time Frame: 2 hours
|
Feeling sick VAS assesses the effect experienced by the participant on a 100 mm unipolar VAS, where responses are unidirectional and range from a response of 'not at all' (score of 0 mm) to 'extremely' (score of 100 mm).
AUE (0-2) = Area under the effect versus time curve from time zero to time of last quantifiable effect (0-2).
|
2 hours
|
|
Feeling Sick: Area Under Effect Curve (AUE) From 0-3 Hours
Time Frame: 3 hours
|
Feeling sick VAS assesses the effect experienced by the participant on a 100 mm unipolar VAS, where responses are unidirectional and range from a response of 'not at all' (score of 0 mm) to 'extremely' (score of 100 mm).
AUE (0-3) = Area under the effect versus time curve from time zero to time of last quantifiable effect (0-3).
|
3 hours
|
|
Feeling Sick: Area Under Effect Curve (AUE) From 0-12 Hours
Time Frame: 12 hours
|
Feeling sick VAS assesses the effect experienced by the participant on a 100 mm unipolar VAS, where responses are unidirectional and range from a response of 'not at all' (score of 0 mm) to 'extremely' (score of 100 mm).
AUE (0-12) = Area under the effect versus time curve from time zero to time of last quantifiable effect (0-12).
|
12 hours
|
|
Nausea: Area Under Effect Curve (AUE) From 0-1 Hour
Time Frame: 1 hour
|
Nausea VAS assesses the effect experienced by the participant on a 100 mm unipolar VAS, where responses are unidirectional and range from a response of 'not at all' (score of 0 mm) to 'extremely' (score of 100 mm).
AUE (0-1) = Area under the effect versus time curve from time zero to time of last quantifiable effect (0-1).
|
1 hour
|
|
Nausea: Area Under Effect Curve (AUE) From 0-2 Hours
Time Frame: 2 hours
|
Nausea VAS assesses the effect experienced by the participant on a 100 mm unipolar VAS, where responses are unidirectional and range from a response of 'not at all' (score of 0 mm) to 'extremely' (score of 100 mm).
AUE (0-2) = Area under the effect versus time curve from time zero to time of last quantifiable effect (0-2).
|
2 hours
|
|
Nausea: Area Under Effect Curve (AUE) From 0-3 Hours
Time Frame: 3 hours
|
Nausea VAS assesses the effect experienced by the participant on a 100 mm unipolar VAS, where responses are unidirectional and range from a response of 'not at all' (score of 0 mm) to 'extremely' (score of 100 mm).
AUE (0-3) = Area under the effect versus time curve from time zero to time of last quantifiable effect (0-3).
|
3 hours
|
|
Nausea: Area Under Effect Curve (AUE) From 0-12 Hours
Time Frame: 12 hours
|
Nausea VAS assesses the effect experienced by the participant on a 100 mm unipolar VAS, where responses are unidirectional and range from a response of 'not at all' (score of 0 mm) to 'extremely' (score of 100 mm).
AUE (0-12) = Area under the effect versus time curve from time zero to time of last quantifiable effect (0-12).
|
12 hours
|
|
Sleepy: Area Under Effect Curve (AUE) From 0-1 Hour
Time Frame: 1 hour
|
Sleepy VAS assesses the effect experienced by the participant on a 100 mm unipolar VAS, where responses are unidirectional and range from a response of 'not at all' (score of 0 mm) to 'extremely' (score of 100 mm).
AUE (0-1) = Area under the effect versus time curve from time zero to time of last quantifiable effect (0-1).
|
1 hour
|
|
Sleepy: Area Under Effect Curve (AUE) From 0-2 Hours
Time Frame: 2 hours
|
Sleepy VAS assesses the effect experienced by the participant on a 100 mm unipolar VAS, where responses are unidirectional and range from a response of 'not at all' (score of 0 mm) to 'extremely' (score of 100 mm).
AUE (0-2) = Area under the effect versus time curve from time zero to time of last quantifiable effect (0-2).
|
2 hours
|
|
Sleepy: Area Under Effect Curve (AUE) From 0-3 Hours
Time Frame: 3 hours
|
Sleepy VAS assesses the effect experienced by the participant on a 100 mm unipolar VAS, where responses are unidirectional and range from a response of 'not at all' (score of 0 mm) to 'extremely' (score of 100 mm).
AUE (0-3) = Area under the effect versus time curve from time zero to time of last quantifiable effect (0-3).
|
3 hours
|
|
Sleepy: Area Under Effect Curve (AUE) From 0-12 Hour
Time Frame: 12 hours
|
Sleepy VAS assesses the effect experienced by the participant on a 100 mm unipolar VAS, where responses are unidirectional and range from a response of 'not at all' (score of 0 mm) to 'extremely' (score of 100 mm).
AUE (0-12) = Area under the effect versus time curve from time zero to time of last quantifiable effect (0-12).
|
12 hours
|
|
Dizzy: Area Under Effect Curve (AUE) From 0-1 Hour
Time Frame: 1 hour
|
Dizzy VAS assesses the effect experienced by the participant on a 100 mm unipolar VAS, where responses are unidirectional and range from a response of 'not at all' (score of 0 mm) to 'extremely' (score of 100 mm).
AUE (0-1) = Area under the effect versus time curve from time zero to time of last quantifiable effect (0-1).
|
1 hour
|
|
Dizzy: Area Under Effect Curve (AUE) From 0-2 Hours
Time Frame: 2 hours
|
Dizzy VAS assesses the effect experienced by the participant on a 100 mm unipolar VAS, where responses are unidirectional and range from a response of 'not at all' (score of 0 mm) to 'extremely' (score of 100 mm).
AUE (0-2) = Area under the effect versus time curve from time zero to time of last quantifiable effect (0-2).
|
2 hours
|
|
Dizzy: Area Under Effect Curve (AUE) From 0-3 Hours
Time Frame: 3 hours
|
Dizzy VAS assesses the effect experienced by the participant on a 100 mm unipolar VAS, where responses are unidirectional and range from a response of 'not at all' (score of 0 mm) to 'extremely' (score of 100 mm).
AUE (0-3) = Area under the effect versus time curve from time zero to time of last quantifiable effect (0-3).
|
3 hours
|
|
Dizzy: Area Under Effect Curve (AUE) From 0-12 Hours
Time Frame: 12 hours
|
Dizzy VAS assesses the effect experienced by the participant on a 100 mm unipolar VAS, where responses are unidirectional and range from a response of 'not at all' (score of 0 mm) to 'extremely' (score of 100 mm).
AUE (0-12) = Area under the effect versus time curve from time zero to time of last quantifiable effect (0-12).
|
12 hours
|
|
Bad Effects: Peak Effect (Emax)
Time Frame: 12 hours
|
Bad effects visual analogue scale (VAS) assesses the effect experienced by the participant on a 100 mm unipolar VAS, where responses are unidirectional and range from a response of 'not at all' (score of 0 mm) to 'extremely' (score of 100 mm).
|
12 hours
|
|
Nausea: Peak Effect (Emax)
Time Frame: 12 hours
|
Nausea visual analogue scale (VAS) assesses the effect experienced by the participant on a 100 mm unipolar VAS, where responses are unidirectional and range from a response of 'not at all' (score of 0 mm) to 'extremely' (score of 100 mm).
|
12 hours
|
|
Feel Sick: Peak Effect (Emax)
Time Frame: 12 hours
|
Feel sick visual analogue scale (VAS) assesses the effect experienced by the participant on a 100 mm unipolar VAS, where responses are unidirectional and range from a response of 'not at all' (score of 0 mm) to 'extremely' (score of 100 mm).
|
12 hours
|
|
Sleepy: Peak Effect (Emax)
Time Frame: 12 hours
|
Sleepy visual analogue scale (VAS) assesses the effect experienced by the participant on a 100 mm unipolar VAS, where responses are unidirectional and range from a response of 'not at all' (score of 0 mm) to 'extremely' (score of 100 mm).
|
12 hours
|
|
Dizzy: Peak Effect (Emax)
Time Frame: 12 hours
|
Dizzy visual analogue scale (VAS) assesses the effect experienced by the participant on a 100 mm unipolar VAS, where responses are unidirectional and range from a response of 'not at all' (score of 0 mm) to 'extremely' (score of 100 mm).
|
12 hours
|
|
Pupillometry: Peak Effect (Emax)
Time Frame: 12 hours
|
Pupillometry assessments measured change in pupil size (miosis) as an indicator of opioid pharmacological properties.
The same eye for each participant was used for all measurements during the study.
Participants had the size of their pupil measured (in mm) using a pupillometer.
Measurements were made in a dimly lit (mesopic) room with controlled lighting conditions.
|
12 hours
|
|
Good Drug Effects: Peak Effect (Emax)
Time Frame: 12 hours
|
Good drug effects VAS assesses the effect experienced by the participant on a 100 mm unipolar VAS, where responses are unidirectional and range from a response of 'not at all' (score of 0 mm) to 'extremely' (score of 100 mm).
AUE (0-12) = Area under the effect versus time curve from time zero to time of last quantifiable effect (0-12).
|
12 hours
|
|
Drug Liking: Area Under Effect Curve (AUE) From 0-1 Hour
Time Frame: 1 hour
|
Drug liking assesses the degree that a participant likes a drug effect at the time the question is being asked (that is, at the moment).
It is scored using a 100 mm unipolar visual analogue scale (VAS), where responses are unidirectional and range from a response of 'not at all' (score of 0 mm) to 'extremely' (score of 100 mm).
|
1 hour
|
|
Drug Liking: Area Under Effect Curve (AUE) From 0-3 Hours
Time Frame: 3 hours
|
Drug liking assesses the degree that a participant likes a drug effect at the time the question is being asked (that is, at the moment).
It is scored using a 100 mm unipolar visual analogue scale (VAS), where responses are unidirectional and range from a response of 'not at all' (score of 0 mm) to 'extremely' (score of 100 mm).
|
3 hours
|
|
Drug Liking: Area Under Effect Curve (AUE) From 0-12 Hours
Time Frame: 12 hours
|
Drug liking assesses the degree that a participant likes a drug effect at the time the question is being asked (that is, at the moment).
It is scored using a 100 mm unipolar visual analogue scale (VAS), where responses are unidirectional and range from a response of 'not at all' (score of 0 mm) to 'extremely' (score of 100 mm).
|
12 hours
|
|
Drug Liking: Time to Maximum (Peak) Effect (TEmax)
Time Frame: 12 hours
|
Drug liking assesses the degree that a participant likes a drug effect at the time the question is being asked (that is, at the moment).
It is scored using a 100 mm unipolar visual analogue scale (VAS), where responses are unidirectional and range from a response of 'not at all' (score of 0 mm) to 'extremely' (score of 100 mm).
|
12 hours
|
|
High: Time to Maximum (Peak) Effect (TEmax)
Time Frame: 12 hours
|
High VAS assesses the effect experienced by the participant on a 100 mm unipolar VAS, where responses are unidirectional and range from a response of 'not at all' (score of 0 mm) to 'extremely' (score of 100 mm).
TEmax = Time to maximum observed score.
|
12 hours
|
|
Any Drug Effects: Time to Maximum (Peak) Effect (TEmax)
Time Frame: 12 hours
|
Any drug effects VAS assesses the effect experienced by the participant on a 100 mm unipolar VAS, where responses are unidirectional and range from a response of 'not at all' (score of 0 mm) to 'extremely' (score of 100 mm).
TEmax = Time to maximum observed score.
|
12 hours
|
|
Good Drug Effects: Time to Maximum (Peak) Effect (TEmax)
Time Frame: 12 hours
|
Good drug effects VAS assesses the effect experienced by the participant on a 100 mm unipolar VAS, where responses are unidirectional and range from a response of 'not at all' (score of 0 mm) to 'extremely' (score of 100 mm).
TEmax = Time to maximum observed score.
|
12 hours
|
|
Bad Drug Effects: Time to Maximum (Peak) Effect (TEmax)
Time Frame: 12 hours
|
Bad drug effects VAS assesses the effect experienced by the participant on a 100 mm unipolar VAS, where responses are unidirectional and range from a response of 'not at all' (score of 0 mm) to 'extremely' (score of 100 mm).
TEmax = Time to maximum observed score.
|
12 hours
|
|
Feel Sick: Time to Maximum (Peak) Effect (TEmax)
Time Frame: 12 hours
|
Feel sick VAS assesses the effect experienced by the participant on a 100 mm unipolar VAS, where responses are unidirectional and range from a response of 'not at all' (score of 0 mm) to 'extremely' (score of 100 mm).
TEmax = Time to maximum observed score.
|
12 hours
|
|
Nausea: Time to Maximum (Peak) Effect (TEmax)
Time Frame: 12 hours
|
Nausea VAS assesses the effect experienced by the participant on a 100 mm unipolar VAS, where responses are unidirectional and range from a response of 'not at all' (score of 0 mm) to 'extremely' (score of 100 mm).
TEmax = Time to maximum observed score.
|
12 hours
|
|
Sleepy: Time to Maximum (Peak) Effect (TEmax)
Time Frame: 12 hours
|
Sleepy visual analogue scale (VAS) assesses the effect experienced by the participant on a 100 mm unipolar VAS, where responses are unidirectional and range from a response of 'not at all' (score of 0 mm) to 'extremely' (score of 100 mm).
|
12 hours
|
|
Dizzy: Time to Maximum (Peak) Effect (TEmax)
Time Frame: 12 hours
|
Dizzy VAS assesses the effect experienced by the participant on a 100 mm unipolar VAS, where responses are unidirectional and range from a response of 'not at all' (score of 0 mm) to 'extremely' (score of 100 mm).
TEmax = Time to maximum observed score.
|
12 hours
|
|
Pupillometry: Time to Maximum (Peak) Effect (TEmax)
Time Frame: 12 hours
|
Pupillometry assessments measured change in pupil size (miosis) as an indicator of opioid pharmacological properties.
The same eye for each participant was used for all measurements during the study.
Participants had the size of their pupil measured (in mm) using a pupillometer.
Measurements were made in a dimly lit (mesopic) room with controlled lighting conditions.
TEmax = Time to maximum observed score.
|
12 hours
|
|
Any Drug Effects: Peak Effect (Emax)
Time Frame: 12 hours
|
Any drug effects VAS assesses the effect experienced by the participant on a 100 mm unipolar VAS, where responses are unidirectional and range from a response of 'not at all' (score of 0 mm) to 'extremely' (score of 100 mm).
|
12 hours
|
|
Texture: Subjective Experience from Chewing
Time Frame: 5 mins
|
Subjective Experience from Chewing is a visual analogue scale (VAS) subjective assessment of the texture of the substance being chewed.
Participants are asked to describe the the texture of the drug using a VAS with score ranging from 0 mm to 100 mm (score of 0 mm = Extremely unpleasant, 50 mm = neutral, and 100 mm = Extremely pleasant).
|
5 mins
|
|
Maximum Observed Plasma Concentration (Cmax)
Time Frame: 24hr
|
24hr
|
|
|
Time to Reach Maximum Observed Plasma Concentration (Tmax)
Time Frame: 24hr
|
24hr
|
|
|
Area under the curve (AUC)
Time Frame: 24hr
|
24hr
|
|
|
Systemic Clearance (CL)
Time Frame: 24hr
|
24hr
|
|
|
volume of distribution (Vd)
Time Frame: 24hr
|
24hr
|
|
|
Half-Life (t1/2)
Time Frame: 24 hours
|
24 hours
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
November 1, 2013
Primary Completion (Actual)
August 1, 2014
Study Completion (Actual)
August 1, 2014
Study Registration Dates
First Submitted
November 1, 2013
First Submitted That Met QC Criteria
November 11, 2013
First Posted (Estimate)
November 18, 2013
Study Record Updates
Last Update Posted (Estimate)
April 4, 2016
Last Update Submitted That Met QC Criteria
March 31, 2016
Last Verified
March 1, 2016
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- B4501016
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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