Screening of Susceptibility Genes in Postoperative Cognitive Dysfunction(POCD)

August 14, 2014 updated by: HailongDong, Xijing Hospital

Screening of Susceptibility Genes in Postoperative Cognitive Dysfunction After On-pump Cardiac Surgery

The aim of this study is to perform a whole-genome linkage analysis for identification of the susceptibility loci for POCD

Study Overview

Status

Unknown

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

Observational

Enrollment (Anticipated)

120

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Shaanxi
      • Xi'an, Shaanxi, China, 710032
        • Recruiting
        • Xijing Hospital
        • Principal Investigator:
          • Hailong Dong, MD, PhD

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

60 years to 75 years (ADULT, OLDER_ADULT)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Probability Sample

Study Population

Old patient(>60 y) who are schedule to receive of-pump cardiac surgery.

Description

Inclusion Criteria:

  1. Age from 60 to 75 years old;
  2. Schedule for on-pump cardiac surgery;
  3. undergoing full intravenous anesthesia;
  4. without hepatic, renal, pulmonary disease or full intravenous anesthesia surgery history;
  5. Gave the informed consent.

Exclusion Criteria:

  1. Emergency surgery;
  2. A history of cerebrovascular disease;
  3. The history of mental disease;
  4. Long term use of sedative and antidepressant drugs;
  5. Alcoholism;
  6. serious vision, hearing impairment and inapprehensive language;
  7. chromosomal abnormalities;
  8. blood disease;
  9. refused to sign the informed consent.

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
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.
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

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
about 10 minutes before anesthesia induction

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
one day before surgery, 7 d after surgery

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

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)

September 1, 2014

Study Completion (Anticipated)

September 1, 2014

Study Registration Dates

First Submitted

March 4, 2014

First Submitted That Met QC Criteria

March 6, 2014

First Posted (Estimate)

March 11, 2014

Study Record Updates

Last Update Posted (Estimate)

August 15, 2014

Last Update Submitted That Met QC Criteria

August 14, 2014

Last Verified

August 1, 2014

More Information

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.

Clinical Trials on Cardiac Surgery Patients

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