- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01881802
Study of Opioid Immunosuppressive Effects
June 19, 2013 updated by: Xiaohong Long, Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University
This trial aims to investigate the effects of opioid-inducing immune suppression on opioid drug abused patients.
The methods of the investigators research mainly includes the expression of morphine-related miRNAs in peripheral blood mononuclear cells and cytokine in plasma.
Study Overview
Status
Unknown
Conditions
Study Type
Observational
Enrollment (Anticipated)
50
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 55 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Guangzhou Psychiatric Hospital
Description
Inclusion Criteria:
- subjects were excluded if they had a chronic systemic illness (cardiac, renal, pulmonary, hepatic, endocrine, metabolic, or autoimmune disorders) or
- a major psychiatric disorder or
- if they were abusing substances other than heroin (as determined by urine drug test result). For women, pregnancy was also a reason for exclusion.
Exclusion Criteria:
- Control subjects with no history of drug or alcohol abuse were also excluded if they had
- major medical or psychiatric disorders
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
---|
morphine or heroin dependence patients
|
normal control group
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
real-time quantitative polymerase chain reaction
Time Frame: up to 2 months
|
up to 2 months
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
enzyme-linked immuno sorbent assay
Time Frame: up to 2 months
|
up to 2 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
March 1, 2013
Primary Completion (Anticipated)
June 1, 2013
Study Registration Dates
First Submitted
June 3, 2013
First Submitted That Met QC Criteria
June 19, 2013
First Posted (Estimate)
June 20, 2013
Study Record Updates
Last Update Posted (Estimate)
June 20, 2013
Last Update Submitted That Met QC Criteria
June 19, 2013
Last Verified
June 1, 2013
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 01 (Miami VAHS)
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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