Comparison of Transthoracic Electrical Bioimpedance and Pulse Contour Analysis in Renal Transplantation Patients

June 17, 2019 updated by: Dita Aditianingsih

Comparison of Transthoracic Electrical Bioimpedance and Pulse Contour Analysis in Renal Transplantation Patients: Analysis of Intraoperative Cardiac Output, Systemic Vascular Resistant and Stroke Volume Variation

Hemodynamics monitoring using non-invasive transthoracic electrical bioimpedance ICON are compatible with standard invasive monitoring using pulse contour analysis EV1000

Study Overview

Study Type

Observational

Enrollment (Actual)

50

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

    • DKI Jakarta
      • Jakarta Pusat, DKI Jakarta, Indonesia, 10430
        • Rumah Sakit Cipto Mangunkusumo

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

18 years to 80 years (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

Patients planned to undergo elective kidney transplantation surgery as recipient

Description

Inclusion Criteria:

  • BMI 18.5 - 35 kg/m^2

Exclusion Criteria:

  • Heart function abnormalities (arrhythmia, AV block, using pacemaker, severe aorta stenosis)
  • Morbid obesity
  • Bradycardia (< 50 bpm)
  • Tachycardia (> 110 bpm)
  • refuse to participate

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

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Hemodynamic correlation
Time Frame: Intraoperative
Correlation between hemodynamic measured between devices: cardiac index, stroke volume index, systemic vascular resistance index, stroke volume index
Intraoperative

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Changes in hemodynamic profiles: Cardiac Index
Time Frame: Intraoperative
The trends of perioperative hemodynamic profiles during and after surgery: cardiac index in L/minutes/m^2
Intraoperative
Changes in hemodynamic profiles: Stroke Volume Index
Time Frame: Intraoperative
The trends of perioperative haemodynamic profiles during and after surgery: stroke volume index in mL/beat/m^2
Intraoperative
Changes in hemodynamic profiles: Systemic Vascular Resistance Index
Time Frame: Intraoperative
The trends of perioperative haemodynamic profiles during and after surgery: systemic vascular resistance index in dynes-second-m^2/cm^5
Intraoperative
Changes in hemodynamic profiles: Stroke Volume Variation
Time Frame: Intraoperative
The trends of perioperative haemodynamic profiles during and after surgery: stroke volume variation in %
Intraoperative

Collaborators and Investigators

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

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

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 (Actual)

March 12, 2019

Primary Completion (Actual)

April 12, 2019

Study Completion (Actual)

May 12, 2019

Study Registration Dates

First Submitted

March 26, 2019

First Submitted That Met QC Criteria

March 26, 2019

First Posted (Actual)

March 28, 2019

Study Record Updates

Last Update Posted (Actual)

June 18, 2019

Last Update Submitted That Met QC Criteria

June 17, 2019

Last Verified

June 1, 2019

More Information

Terms related to this study

Other Study ID Numbers

  • IndonesiaUAnes032

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

Yes

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.

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