Double Blind Randomized, Monocentric, Cross-over, Placebo-controlled Study to Evaluate the Effect of Morphine and Naloxone on Motivation (MBBAnalgesic)

NCT ID: NCT02267304

Last Updated: 2021-08-26

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

PHASE2

Total Enrollment

37 participants

Study Classification

INTERVENTIONAL

Study Start Date

2013-10-30

Study Completion Date

2016-08-30

Brief Summary

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The aim of the current study is to examine the role of the opioïd system on the cognitive parameters of motivation. They are embedded in a conceptual framework of motivation that merges decision-making and reinforcement learning theories. Every action is conceived as path from one state to another. The different states are associated to different values (positive for rewards and negative for punishments), and the different actions to different costs (risk, effort and delay). The tasks are designed such that the sensitivity to the state and action parameters can be inferred by fitting computational models.The primary objective is to characterize the effect of Morphine 0,05mg/kg and Naloxone 10mg on cost accumulation slope, assessed in an effort management task, in which participants are asked to squeeze a hand grip during 30 seconds at varying level of effort in order to win monetary payoff. Secondary objectives are to characterize the effect of Morphine 0,05mg/kg and Naloxone 10mg on other cognitive parameters of motivation (assessed with a motivational battery that includes rating, choice and learning tasks).

Detailed Description

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Conditions

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Healthy

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

SINGLE_GROUP

Primary Study Purpose

OTHER

Blinding Strategy

TRIPLE

Participants Caregivers Investigators

Study Groups

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Morphine/placebo/naxolone

Group Type EXPERIMENTAL

50 mL of sodium chloride (0,9%)

Intervention Type DRUG

Morphine 0,05mg/kg

Intervention Type DRUG

Naloxone 10mg

Intervention Type DRUG

Naxolone/morphine/placebo

Group Type EXPERIMENTAL

50 mL of sodium chloride (0,9%)

Intervention Type DRUG

Morphine 0,05mg/kg

Intervention Type DRUG

Naloxone 10mg

Intervention Type DRUG

placebo/naxolone/morphine

Group Type EXPERIMENTAL

50 mL of sodium chloride (0,9%)

Intervention Type DRUG

Morphine 0,05mg/kg

Intervention Type DRUG

Naloxone 10mg

Intervention Type DRUG

Interventions

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50 mL of sodium chloride (0,9%)

Intervention Type DRUG

Morphine 0,05mg/kg

Intervention Type DRUG

Naloxone 10mg

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

* Man or woman, age ≥ 18 and \< 50
* Weight between 50 kg and 90 kg.
* No contraindication to effort
* No evolutive pathology that could interfere with the current study signed consent
* medical insurance ("sécurité sociale")

Exclusion Criteria

* Age \< 18 or \> 50
* Smokers
* Person under curatorship, or guardianship, or with civil rights deprivation
* History of neurologic or psychiatric pathology
* Chronic or actual consumption of alcohol, or psychotropic drugs
* pregnancy, breastfeeding
* Woman of childbearing potential without effective contraception
* Liver failure
* Severe Cardiovascular Disorders
* Severe Cerebrovascular Discorders
* Morphine (or Naloxone) hypersensitivity/addiction
* Treatment contraindicated: morphine dérivatives, neuroleptics, barbiturate, benzodiazepine, anxiolytics, hypnotics, antidepressant, antihistamine, antihypertensives, beta blocker, baclofen, thalidomide
* Enzyme inducers, (rifampicine, …)
* Treatment that can interfere with the performance of the subject: beta2 adrenergic agonists, analgesics, corticosteroïds, anti-inflammatory drugs, …
Minimum Eligible Age

18 Years

Maximum Eligible Age

50 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Institut National de la Santé Et de la Recherche Médicale, France

OTHER_GOV

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Jean -Christophe Corvol, MCU-PH

Role: PRINCIPAL_INVESTIGATOR

CIC Neurologie GH Pitié Salpêtrière

Locations

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CIC Neurologie GHPS

Paris, , France

Site Status

Countries

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France

Other Identifiers

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2013-003487-31

Identifier Type: EUDRACT_NUMBER

Identifier Source: secondary_id

C13-02

Identifier Type: -

Identifier Source: org_study_id

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