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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02637076
Other study ID # 017-2014
Secondary ID
Status Completed
Phase Phase 4
First received
Last updated
Start date January 2016
Est. completion date January 23, 2020

Study information

Verified date February 2021
Source Centre for Addiction and Mental Health
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The overall aim of this investigation is to establish whether an action of Xyrem® on the brain dopamine system in patients with narcolepsy, and in a comparison control group, might explain part of the anti-narcoleptic effect of the drug. Trial Objective is to establish, using positron emission tomography (PET), in Xyrem®-naïve narcolepsy with cataplexy patients, and in matched controls, whether a single dose of Xyrem® causes changes in striatal binding of 11C-raclopride and 11C-DTBZ that would suggest altered activity of brain dopamine neurones.


Recruitment information / eligibility

Status Completed
Enrollment 17
Est. completion date January 23, 2020
Est. primary completion date January 23, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 19 Years and older
Eligibility Inclusion Criteria: - current diagnosis of narcolepsy with cataplexy OR healthy control Exclusion Criteria: - use of any sedative hypnotics, tranquilizers, anticonvulsants, antihistamines (except non-sedating), benzodiazepines, clonidine or any medication known to affect dopamine at start of baseline period - significant unstable or uncontrolled medical/psychiatric disease - significant history of head trauma/surgery or seizure disorder - radiation exposure exceeding 20mSv in last 12 months - pregnancy - substance abuse/dependence (including alcohol) - have sleep apnea, or are shift workers - on a sodium-restricted diet - has ever taken Xyrem / sodium oxybate / GHB at any time - claustrophobia - metal implants / objects in the body that may interfere with MRI - succinic semialdehyde dehydrogenase deficiency

Study Design


Intervention

Drug:
Xyrem
single 3.0 gram dose

Locations

Country Name City State
Canada Centre for Addiction and Mental Health (CAMH) Toronto Ontario

Sponsors (1)

Lead Sponsor Collaborator
Centre for Addiction and Mental Health

Country where clinical trial is conducted

Canada, 

Outcome

Type Measure Description Time frame Safety issue
Primary [C-11]Raclopride BPND at 1 Hour Post Xyrem BPND (Binding Potential) of [C-11]raclopride measures 1 hour after taking a single 3g dose of Xyrem. 1 hour post Xyrem
Primary % Change in PET [C11]Raclopride Binding From Baseline After Single Dose of Xyrem [C-11] raclopride is a radioligand that binds to the D2/3 dopamine receptor in the dopamine-rich striatum and which is sensitive to dopamine occupancy.
% change was calculated as follows: (1 hour BPND - baseline BPND)/baseline BPND *100; Mean % change represents the mean of each participant's individual % change within the group.
1 hour post Xyrem
Primary [C-11]Raclopride BPND at 7 Hours Post Xyrem BPND (Binding Potential) of [C-11]raclopride measures 7 hours after taking a single 3g dose of Xyrem. 7 hours post Xyrem
Primary % Change in PET [C11]Raclopride Binding From Baseline After Single Dose of Xyrem [C-11] raclopride is a radioligand that binds to the D2/3 dopamine receptor in the dopamine-rich striatum and which is sensitive to dopamine occupancy.
% change was calculated as follows: (7 hours BPND - baseline BPND)/baseline BPND *100; Mean % change represents the mean of each participant's individual % change within the group.
7 hours post Xyrem
Secondary [C-11]DTBZ BPND at 5 Hours Post Xyrem Measurement of [C-11]DTBZ 5 hours after taking a single dose of 3g Xyrem 5 hours post single Xyrem dose
Secondary % Change in PET [C-11] Dihydrotetrabenazine (DTBZ) Binding From Baseline to Five Hours Post Xyrem [C-11] DTBZ is a radioligand that binds to the vesicular monoamine transporter and which is sensitive to dopamine occupancy.
% change was calculated as follows: (5 hour BPND - baseline BPND)/baseline BPND *100; Mean % change represents the mean of each participant's individual % change within the group.
5 hours post single Xyrem dose
Secondary Blood Gamma-hydroxybutyrate (GHB) Concentration (AUC) The concentration of gammahydroxybutyrate in blood of participants who have received a single dose of Xyrem, as measured by Area Under the Curve. multiple time points from 0 to 7 hours post-Xyrem
Secondary Blood Gamma-hydroxybutyrate (GHB) Cmax The concentration of gammahydroxybutyrate in blood of participants who have received a single dose of Xyrem as measured by Cmax. multiple time points from 0 to 7 hours post-Xyrem
Secondary Duration of Drowsiness Period of time when the participant was experiencing the sedative action of Xyrem. Data derived from self-report as well as anesthesiologist observation. observed after receiving single dose of Xyrem, up to 9 hours
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