MedPath

The Global QUEST initiative: QUality of life Evaluation STudy:Assessing Health Related Quality of Life in patients receiving medicinal cannabis.

Not Applicable
Recruiting
Conditions
Chronic pain
Multiple Sclerosis
Epilepsy
Parkinson's Disease
Cancer
Cancer - Any cancer
Neurological - Epilepsy
Neurological - Parkinson's disease
Neurological - Multiple sclerosis
Registration Number
ACTRN12623000583640
Lead Sponsor
ittle Green Pharma Ltd
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
12000
Inclusion Criteria

All of the following must be satisfied for enrollment in the study:
•adult patients (aged 18 years)
•patient has been identified as eligible to receive medicinal cannabis by a TGA approved Authorised Prescriber or via the Special Access Scheme (SAS-B) and the doctor has sought and obtained TGA approval for Little Green Pharma (LGP) products for their patient.
•patient is able to read and understand English
•patient is able to provide informed consent
•patient has not started any prescribed medicinal cannabis therapy in the previous 4 weeks; or started prescribed LGP medicinal cannabis therapy within the previous 2 days (we expect no therapeutic benefit within 2 days) and has not received any prescribed medicinal cannabis therapy in the previous 4 weeks
•patient has a life expectancy of more than 3 months .

Exclusion Criteria

Patients will be excluded from the study if any of the following criteria apply:
•are unconscious or confused
•have cognitive impairment
•are pregnant or breastfeeding
•are unable to speak, read and/or write in English
•are denied access to medicinal cannabis under the relevant Special Access Scheme (SAS) for their country of registration
•are unable to provide informed consent
•are already receiving prescribed medicinal cannabis treatment for more than 2 days
•have received prescription medicinal cannabis within the last 4 weeks (excluding previous 2 days)

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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