- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05730140
The Association Between the Intraoperative Blood Pressure Changes and Whole Exome Genome
Association Between Whole Exon Sequencing and Arterial Stiffness in Patients With Intraoperative Hypotension)
Study Overview
Status
Intervention / Treatment
Detailed Description
We aim to elucidate the association between the whole exome genome and intraoperative blood pressure changes.
We will enroll patients older than 20 years old and undergo elective general anesthesia.
Before anesthesia, we will obtain blood sample for whole exome genome test and give arterial line for intraoperative monitor.
After completing surgery, we will follow the patients' all postoperative major organ function.
We hope this study to be able to give us the more information about the specific genetic effect on the arterial stiffness and intraoperative blood pressure changes.
Study Type
Enrollment (Anticipated)
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- elective general surgery
Exclusion Criteria:
- coagulopathy
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
patients undergoing general anesthesia
|
this study did not involve interventions.
This study is an observational study for elucidating the intraoperative blood pressure changes, artierial stiffness, and whole exome genome
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
The association between the arterial stiffness and whole exome genome
Time Frame: 15 minutes
|
using pearson correlation to describe the association
|
15 minutes
|
Collaborators and Investigators
Study record dates
Study Major Dates
Study Start (Anticipated)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- 202209125RINC
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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