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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02771067
Other study ID # 4-2016-0205
Secondary ID
Status Completed
Phase N/A
First received May 4, 2016
Last updated December 15, 2017
Start date September 29, 2016
Est. completion date February 23, 2017

Study information

Verified date December 2017
Source Yonsei University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to investigate the validity of pulse pressure variation to predict fluid responsiveness in patients undergoing robotic or laparoscopic gastrectomy.


Recruitment information / eligibility

Status Completed
Enrollment 30
Est. completion date February 23, 2017
Est. primary completion date February 23, 2017
Accepts healthy volunteers No
Gender All
Age group 19 Years and older
Eligibility Inclusion Criteria:

- adult patients aged over 19 years who are scheduled for robotic or laparoscopic gastrectomy

Exclusion Criteria:

- cardiac arrhythmia

- valvular heart disease

- ischemic heart disease

- left ventricular ejection fraction less than 40%

- Pulmonary disease

- esophageal disease

- upper gastrointestinal bleeding

- Body mass index more than 40 kg/m2.

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Fluid infusion
Fluid infusion will be performed using 6% hydroxyethyl starch. Pulse pressure variation and stroke volume will be measured before and after fluid infusion.

Locations

Country Name City State
Korea, Republic of Department of Anesthesiology and Pain Medicine Anesthesia and Pain Research Institute Yonsei University Seoul

Sponsors (1)

Lead Sponsor Collaborator
Yonsei University

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary Pulse pressure variation Ability of pulse pressure variation to predict fluid responsiveness will be evaluated. During the surgery. At Day 0.
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