- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02084030
Screening of Susceptibility Genes in Postoperative Cognitive Dysfunction(POCD)
Screening of Susceptibility Genes in Postoperative Cognitive Dysfunction After On-pump Cardiac Surgery
Study Overview
Status
Conditions
Detailed Description
BACKGROUND: Postoperative cognitive dysfunction is probably the most frequent type of postoperative cognitive impairment. As it mainly affect the elderly population, POCD is receiving increasing attention. However, the pathophysiology of POCD remains incompletely understood. No study had elucidate why somebody are apt to suffer from POCD, but others not. In current study, we try to use GWAS technology to find out whether there is a correlation between POCD and gene specificity.
DESIGNING: 120 patients will be screened who are schedule to receive selective on-pump cardiac surgery, 5 ml blood of the patient will be collected before anesthesia induction. Investigetors will measure the cognitive function of the patients one day before surgery and 7 d after surgery and identify whether the patient suffer from POCD used in MMSE test. Randomly select 36 patients who suffer from POCD and 36 patients without POCD(control), GWAS technology will be used to screen the susceptibility gene between these two groups.
EXPECTED RESULTS :Find out some susceptibility genes correlate to POCD.
CONCLUSIONS: The patients who are apt to suffer from POCD have some special susceptibility genes differ from normal people.
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Locations
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Shaanxi
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Xi'an, Shaanxi, China, 710032
- Recruiting
- Xijing Hospital
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Principal Investigator:
- Hailong Dong, MD, PhD
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Age from 60 to 75 years old;
- Schedule for on-pump cardiac surgery;
- undergoing full intravenous anesthesia;
- without hepatic, renal, pulmonary disease or full intravenous anesthesia surgery history;
- Gave the informed consent.
Exclusion Criteria:
- Emergency surgery;
- A history of cerebrovascular disease;
- The history of mental disease;
- Long term use of sedative and antidepressant drugs;
- Alcoholism;
- serious vision, hearing impairment and inapprehensive language;
- chromosomal abnormalities;
- blood disease;
- refused to sign the informed consent.
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
|---|
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Experimental: Patient with POCD
Patients who suffer from POCD after surgery.
The mini-mental state examination scale decline more than 1 SD of baseline after surgery.
|
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Sham Comparator: patient without POCD
Patients who don't suffer from POCD after surgery.
There is no obvious difference between pre-operation and post-operation in mini-mental state examination scale
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
single nucleotide polymorphisms(SNPs) of each patient
Time Frame: about 10 minutes before anesthesia induction
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about 10 minutes before anesthesia induction
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
mini-mental state examination scale
Time Frame: one day before surgery, 7 d after surgery
|
the cognitive function
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one day before surgery, 7 d after surgery
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Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- DONG2014POCD
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