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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02207842
Other study ID # P00012751
Secondary ID
Status Completed
Phase N/A
First received July 30, 2014
Last updated April 28, 2017
Start date November 2014
Est. completion date January 2017

Study information

Verified date April 2017
Source Boston Children’s Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

One of the most common side effects of a surgical procedure is infection. In order to lower the number of infections that occur after surgery, it is important for physicians to know how medications used during surgery affect the way the body fights infection. Often, when anesthesiologists are helping people go to sleep before surgery they give people medications known as "volatile anesthetics". Volatile anesthetics are medications that can change from a liquid or solid to a gas very easily. Some studies suggest that these types of medications may change the way white blood cells work in the body. Changing the way white blood cells work could possibly increase the person's risk of infection after their surgery or weaken their body's ability to fight infections. The goal of this research study is to learn about how volatile anesthesia medications change the way white blood cells work in people having anesthesia for cardiac procedures. To do this, investigators will examine the function of while blood cells in the laboratory based setting.


Recruitment information / eligibility

Status Completed
Enrollment 41
Est. completion date January 2017
Est. primary completion date January 2017
Accepts healthy volunteers No
Gender All
Age group 12 Months and older
Eligibility Inclusion Criteria:

- Male and female patients

- greater than or equal to 12 months of age

- scheduled for a cardiac catheterization, cardiac surgery, or cardiac MRI

Exclusion Criteria:

- known underlying hematological disorder

- known oncological disorder

- patients who do not require preoperative laboratory testing

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
United States Boston Children's Hospital Boston Massachusetts

Sponsors (1)

Lead Sponsor Collaborator
Boston Children’s Hospital

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Leukocyte function under anesthesia The study will evaluate ex vivo leukocyte function by testing leukocyte activation, TNF-a production, and phagocytic function in the laboratory. up to 12 months
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