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To compare effectiveness of Lorazepam and Risperidone in the treatment of Cannabis Induced Psychotic Disorder

Not Applicable
Completed
Conditions
Health Condition 1: F129- Cannabis use, unspecified
Registration Number
CTRI/2021/05/033552
Lead Sponsor
Government medical college and hospital Chandigarh
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
40
Inclusion Criteria

Patients fulfilling the diagnostic criteria for cannabis induced psychotic disorder as

per DSM-5.

18-65 years old Male patients.

Patients willing for admission in ward for treatment.

Patients who test positive for cannabinoids on urine screening.

Patients with a reliable informant.

Patients willing to give consent.

Exclusion Criteria

Patients with comorbid dependence on other substances except caffeine and nicotine.

Patients having current comorbid major mental illness.

Patients with a history of medical/physical illness where the use of Lorazepam/

Risperidone is contraindicated. For e.g. chronic liver disease, chronic kidney disease,

chronic lung disease, head injury etc.

History of hypersensitivity to Lorazepam/ Risperidone.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Reduction in the severity of psychopathology as assessed by the administration of various psychiatric rating scales like positive and negative syndrome scale (PANSS) and Young mania rating scale (YMRS) on a daily basis till 10 days after the initiation of treatment.Timepoint: positive and negative syndrome scale (PANSS) and Young mania rating scale (YMRS) shall be administered at baseline and, thereafter, daily for a period of 10 days.
Secondary Outcome Measures
NameTimeMethod
to assess the severity of dependence, evolution of withdrawal symptoms and craving using the severity of dependence scale (SDS), cannabis withdrawal scale (CWS) and marijuana craving questionnaire (MCQ) respectively.Timepoint: severity of dependence scale (SDS) shall be administered at baseline only. cannabis withdrawal scale (CWS) and marijuana craving questionnaire (MCQ) shall be applied at baseline and, thereafter, daily for a period of 10 days.
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