Pharmacokinetic Study of Effect of Cardiac Output on the Uptake of Isoflurane

February 1, 2015 updated by: Rajarajan Ganesan, Postgraduate Institute of Medical Education and Research

Effect of Cardiac Output on Uptake of Isoflurane

This study examines the effect of blood flow through the lungs and the body on the consumption and hence requirement of the anesthetic agent isoflurane.

Study Overview

Status

Completed

Conditions

Detailed Description

The effect of cardiac output on the uptake of isoflurane is yet to be quantified. This study aims to obtain a quantifiable relationship between isoflurane uptake and cardiac output. The study patients will be cardiac patients in whom anesthesia is induced with fentanyl , propofol and maintained on isoflurane . The baseline cardiac index from the pulmonary artery catheter as displayed on the continuous cardiac output monitor will be used to classify the patients into two groups with cardiac index of 2.1 liters per minute per square meter as the differentiating criteria. No change in the anesthesia protocol will be done for the two groups.The study is designed such that all vascular catheterisations and the dose of isoflurane administered is as per prevailing institutional protocols and that no other intervention particular or unique to the study is done. As such the data that the study will use is also routinely acquired during the procedure but not systematically stored, which is what the study will do. This, we suggest, makes the study an observational study.The continuous cardiac output data and the inspired and expired concentration of isoflurane as displayed on the monitor will be recorded online. Data will be collected from the start of isoflurane till 30 minutes or till the surgeon starts cannulating the great vessels. The data so obtained will be analysed in two groups based on the baseline cardiac index using Statistical Package for the Social Sciences (SPSS) for difference in uptake between the groups.

Study Type

Observational

Enrollment (Actual)

33

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

      • Chandigarh, India, 160012
        • Postgraduate Institute of Medical Education and Research

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 60 years (Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

Patients undergoing elective, open cardiac procedures under general endotracheal anesthesia with cardiopulmonary bypass

Description

Inclusion Criteria:

  • Presence of valve stenosis / valvular regurgitant lesion/ coronary artery disease with Ejection fraction >40%
  • Posted for open cardiac surgery under general endotracheal anesthesia

Exclusion Criteria:

  • Shunt lesion
  • Allergy to propofol
  • Psychotropic drug use
  • Preinduction hemodynamic instability

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
Reference
Baseline cardiac index more than or equal to 2.1 liters per minute per square meter
Low cardiac output
Baseline cardiac index less than 2.1 liters per minute per square meter

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
Uptake of isoflurane in milliliter of vapor per minute
Time Frame: Every minute from 1 to 30 minutes
Every minute from 1 to 30 minutes

Collaborators and Investigators

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

Investigators

  • Study Director: GOVERDHAN D PURI, MD,Ph.D, Post Graduate Institute of Medical Education and Research
  • Principal Investigator: Rajarajan Ganesan, M.D., Post Graduate Institute of Medical Education and Research
  • Principal Investigator: Aveek Jayant, M.D.,D.M., Post Graduate Institute of Medical Education and Research
  • Principal Investigator: Shyam Thingnam, M.S., Post Graduate Institute of Medical Education and Research

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.

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

October 1, 2013

Primary Completion (Actual)

December 1, 2014

Study Completion (Actual)

December 1, 2014

Study Registration Dates

First Submitted

January 16, 2015

First Submitted That Met QC Criteria

January 27, 2015

First Posted (Estimate)

January 30, 2015

Study Record Updates

Last Update Posted (Estimate)

February 3, 2015

Last Update Submitted That Met QC Criteria

February 1, 2015

Last Verified

February 1, 2015

More Information

Terms related to this study

Other Study ID Numbers

  • 9151/PG-2Trg/2012

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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