The Effects of Cannabis Use in People With Schizophrenia on Clinical, Neuropsychological and Physiological Phenotypes

Schizophrenia Clinical Trial

Official title:

The Effects of Cannabis Use in People With Schizophrenia on Clinical, Neuropsychological and Physiological Phenotypes

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT01832766
• Other study ID #: 05-0359
• Status: Terminated
• Phase: Phase 1/Phase 2
• First received: March 25, 2013
• Last updated: August 18, 2015
• Start date: June 2005
• Est. completion date: May 2011

Study information

• Verified date: August 2015
• Source: University of Colorado, Denver
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Data and Safety Monitoring Board
• Study type: Interventional

Clinical Trial Summary

Approximately 25% of people with schizophrenia abuse marijuana. These people may be using marijuana to self-medicate symptoms such as hallucinations (hearing or seeing things that are not heard or seen by others) or delusions (false beliefs i.e. people are harassing or persecuting them) or the depressed and anxious feelings brought on by these symptoms. Currently, it is unknown whether marijuana makes schizophrenia better or worse. Marijuana intoxication in people without schizophrenia generally causes decreased recall of words, may decrease reaction time and decrease inhibition. Additionally, marijuana may cause distractibility as demonstrated by difficulty keeping their eyes on a moving target and difficulty inhibiting their response to repetitive tones. However, marijuana may have different effects in schizophrenia. Receptors for cannabis (marijuana) are concentrated in the brain and maladjustment of the cannabinoid system may be associated with the difficulty in thinking found in schizophrenia. The proposed research project examines if clinical symptoms, learning, memory, inhibition and distractibility are improved or made worse by the acute ingestion of tetrahydrocannabinol (THC).

Description:

The trial will be a double two period (visit) blind cross-over trial with one arm dronabinol 10 mg one arm a placebo control. The order of doses and placebo will be randomized with the restriction that half of the subjects will receive each order. This counterbalances possible visit effects or learning effects associated with the visits. The use of an oral cannabis analog is not equivalent to smoking as the onset of action is slower. This is why people who use dronabinol for chronic pain prefer to smoke cannabis. There is no "high" associated with dronabinol. However, the active ingredients are the same, THC, which will have similar effects on the cannabinoid 1 receptor. Ethically, we did not feel we could ask people to smoke cannabis on one day of study. Subjects will present to the GCRC at 5:00 p.m. They will abstain from use of cannabis overnight. The following morning, at 8:00 a.m., the subject will provide a urine sample for a toxicology screen and a blood sample for quantitative THC levels. They will then be administered either 10 mg of dronabinol or an identical placebo on an alternate day. The subject will then have a baseline assessment of clinical positive and negative symptoms measured by the Brief Psychiatric Rating Scale (BPRS). The majority (70-90%) of people with schizophrenia smoke cigarettes. Thus, it is likely that in this population that smokes cannabis, 100% will also be cigarette smokers. The effects of nicotine via cigarette smoking on the endophenotypes studied is an acute effect, with a peak at about 5 minutes. To preclude nicotine effects on endophenotypes, we have the patient not smoke for 20 minutes prior to and during testing. Nicotine is quickly removed from the body when inhaled and its effects wear off within 20 minutes. Two hours after administration, the subject will perform the following tests: P50 auditory evoked potential- the recording will consist of the presentation of 5 sets of 16 click pairs with an intrapair interval of 500 ms heard through headphones with a 3-minute rest between sets. Brain wave responses will be recorded; neurocognitive assessment-the California Verbal Learning Test will measure verbal memory and the Stroop will measure inhibition; clinical symptom assessment- The BPRS will again be administered measure positive and negative symptoms; and a blood sample will be collected for quantitative THC levels. They will then be escorted by a Clinical Research Center nurse over to a laboratory at Colorado Psychiatric Hospital to perform smooth pursuit eye movements In performing smooth pursuit eye movements, they will watch a dot moving across a computer screen while infrared sensors that are placed just in front of their eyes record their eye movements. Each subject performs 3 trials of one minute each, with 2 minutes rest between each recording. Subjects will be reassessed by the BPRS for drug exacerbation of symptoms, will have vitals, will be checked for adverse effects, will perform a sobriety test (the standard test used in roadside testing i.e. walking a straight line and finger to nose testing) which will be assessed by Dr. Olincy, who is experienced in assessing sobriety, to assure that the patient is not acutely intoxicated and able to perform normal functions that require coordination. If they fail the sobriety test, they will be asked to remain in the (General Clinical Research Center (GCRC) until they can pass the sobriety test. Otherwise, they will then will be discharged at 5:00 p.m. Transportation to and from the GCRC will be by a provided cab service. Subjects will be randomized in blocks of 4 or 6 to the order in which they receive placebo or dronabinol. The interval between the two days of testing will be 1 week.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 13
• Est. completion date: May 2011
• Est. primary completion date: May 2010
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years to 50 Years

Eligibility

Inclusion Criteria:

• Male and females

• 18 and 50 years of age

• Diagnosis of schizophrenia

• Chronic cannabis users who have used for at least 1 year

• Using cannabis at least once weekly

• Currently being treated with antipsychotic medication

• Must be on a the same dose of antipsychotic medication for at least 3 months.

• Females of childbearing potential must use an adequate form of birth control while participating.

• Participants will be required to have blood pressures greater than 90/60 and less than 140/90.

Exclusion Criteria:

• Use of illicit drugs other than cannabis

• Any psychiatric hospitalizations within 3 months

• pregnancy in females

• taking clozapine

Study Design

Allocation: Randomized, Intervention Model: Crossover Assignment, Masking: Double Blind (Subject, Investigator, Outcomes Assessor)

Related Conditions & MeSH terms

• Schizophrenia

Intervention

Drug:
• Dronabinol
dronabinol 10 mg one capsule by mouth at 8:00 a.m.

Other:
• Placebo Comparator
one capsule given by mouth at 8:00 a.m.

Locations

Country	Name	City	State
United States	University of Colorado Denver	Aurora	Colorado

Sponsors (2)

Lead Sponsor	Collaborator
University of Colorado, Denver	National Alliance for Research on Schizophrenia and Depression

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Brief Psychiatric Rating Scale Change From Baseline at 1 Hour	Measures psychiatric symptoms. Each item is scored from 1-7. Positive symptoms are calculated from sum of scores on hallucinatory behavior, unusual thought content and conceptual disorganization. Thus, the range of Total Positive Symptoms can be from a score of 3-21 .The higher the score, the more severe the symptom. Negative symptoms have been calculated from sum of blunted affect, emotional withdrawal and motor retardation. The range of Total Negative Symptoms can be from a score of 3-21. The higher the score, the more severe the symptoms. As this is a difference from baseline, there can be either negative or positive results as the subjects can either be better than baseline (positive score) or worse than baseline (negative score).	at 1 hour after drug administration	No
Primary	P50 Auditory Evoked Potential	electrophysiological measure of ability to filter extraneous stimuli measured as the amplitude of the evoked response to the second auditory stimulus divided by the amplitude of the evoked response to the first auditory stimulus in mV.	2 hours after drug administration	No
Secondary	California Verbal Learning Test Change at 2 Hours From Baseline	ability to remember a list of words given 5 trials. Number of words remembered is normalized to a schizophrenia population and average scores are calculated with age correction. The normal T-score is 50 and scores greater than 50 correspond with greater ability to remember words as compared to a schizophrenia population norm.	2 hours after drug administration	No