- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02351557
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
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Chandigarh, India, 160012
- Postgraduate Institute of Medical Education and Research
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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 |
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Reference
Baseline cardiac index more than or equal to 2.1 liters per minute per square meter
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Low cardiac output
Baseline cardiac index less than 2.1 liters per minute per square meter
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
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Uptake of isoflurane in milliliter of vapor per minute
Time Frame: Every minute from 1 to 30 minutes
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Every minute from 1 to 30 minutes
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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.
General Publications
- Watt SJ, Cook LB, Ohri S, Lockwood GG. The relationship between anaesthetic uptake and cardiac output. Anaesthesia. 1996 Jan;51(1):24-8. doi: 10.1111/j.1365-2044.1996.tb07648.x.
- Myles PS, Storer R, Millar C. Haemodynamic effects and uptake of enflurane in patients undergoing cardiac surgery: good versus poor myocardial function. Anaesth Intensive Care. 1992 Feb;20(1):21-7. doi: 10.1177/0310057X9202000104.
- Kennedy RR, Baker AB. The effect of cardiac output changes on end-expired volatile anaesthetic concentrations--a theoretical study. Anaesthesia. 2001 Nov;56(11):1034-40. doi: 10.1046/j.1365-2044.2001.02212.x.
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.