Comparison of TIVA by Closed Loop Anaesthesia Delivery System Versus Target Controlled Infusion Device
Evaluation of Propofol Total Intravenous Anaesthesia Administered by Closed Loop Anaesthesia Delivery System Versus Target Controlled Infusion Device in Adults Undergoing Non-Cardiac Surgery: A Randomised Controlled Study
Study Overview
Status
Status
Conditions
Conditions
Intervention / Treatment
Intervention / Treatment
Detailed Description
Study Type
Study Type
Enrollment (Actual)
Enrollment
Phase
Phase
- Not Applicable
Contacts and Locations
Study Contact
Study Contact
- Name: Nitin Sethi, MBBS, DNB
- Phone Number: 00911142252523
- Email: nitinsethi77@yahoo.co.in
Study Contact Backup
- Name: Amitabh Dutta, MBBS, MD, PGDHR
- Phone Number: 00911142252523
- Email: duttaamitabh@yahoo.com
Study Locations
-
-
Delhi
-
New Delhi, Delhi, India, 110060
- Sir Ganga Ram Hospital
-
New Delhi, Delhi, India, 110060
- Nitin Sethi
-
-
Participation Criteria
Eligibility Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- aged 18-65 years
- ASA physical status I-II
- undergoing elective non-cardiac surgery of minimum 60-minutes duration
Exclusion Criteria:
- Uncompensated cardiovascular disease (e.g. uncontrolled hypertension, atrio-ventricular block, sinus bradycardia, congenital heart disease, reduced LV compliance, diastolic dysfunction)
- Hepato-renal insufficiency
- Uncontrolled endocrinology disease (e.g. diabetes mellitus, hypothyroidism)
- Known allergy/hypersensitivity to the study drug
- Drug dependence/substance abuse
- Requirement of postoperative ventilation
- Refusal to informed consent
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Number of Arms
Arms and Interventions
Participant Group / ArmParticipant Group / Arm |
Intervention / TreatmentIntervention / Treatment |
|---|---|
|
Active Comparator: CLADS group
Propofol administration rate will be controlled by a feedback loop facilitated by BIS monitoring using the closed-loop anaesthesia delivery system (CLADS).
A BIS value of 50 will be used as the target point for induction and maintenance of anesthesia.
|
Propofol administration rate will be controlled by a feedback loop facilitated by BIS monitoring using the closed loop anaesthesia delivery system (CLADS).
A BIS value of 50 will be used as the target point for induction and maintenance of anaesthesia.
The target controlled infusion (TCI) pump will be programmed to marsh model with the target plasma site concentration of 3-µg/ml.
The plasma concentration will be altered to maintain a target BIS of 50 during induction and maintenance of anesthesia
The target controlled infusion (TCI) pump will be programmed to Schneider model with the target effect site concentration of 3-µg/ml.
The effect-site concentration will be altered to maintain a target BIS of 50 during induction and maintenance of anesthesia
Manual propofol administration will be done using an intravenous infusion pump to maintain a target BIS of 50 during induction and maintenance of anesthesia.
|
|
Active Comparator: Marsh model group
The target-controlled infusion (TCI) pump will be programmed to marsh model with the target plasma site concentration of 3-µg/ml.
The plasma concentration will be altered to maintain a target BIS of 50 during induction and maintenance of anesthesia
|
Propofol administration rate will be controlled by a feedback loop facilitated by BIS monitoring using the closed loop anaesthesia delivery system (CLADS).
A BIS value of 50 will be used as the target point for induction and maintenance of anaesthesia.
The target controlled infusion (TCI) pump will be programmed to marsh model with the target plasma site concentration of 3-µg/ml.
The plasma concentration will be altered to maintain a target BIS of 50 during induction and maintenance of anesthesia
The target controlled infusion (TCI) pump will be programmed to Schneider model with the target effect site concentration of 3-µg/ml.
The effect-site concentration will be altered to maintain a target BIS of 50 during induction and maintenance of anesthesia
Manual propofol administration will be done using an intravenous infusion pump to maintain a target BIS of 50 during induction and maintenance of anesthesia.
|
|
Active Comparator: Schnider model group
The TCI-pump will be programmed to will be programmed to Schnider model with the target effect site concentration of 3-µg/ml.
The effect-site concentration will be altered to maintain a target BIS of 50 during induction and maintenance of anesthesia.
|
Propofol administration rate will be controlled by a feedback loop facilitated by BIS monitoring using the closed loop anaesthesia delivery system (CLADS).
A BIS value of 50 will be used as the target point for induction and maintenance of anaesthesia.
The target controlled infusion (TCI) pump will be programmed to marsh model with the target plasma site concentration of 3-µg/ml.
The plasma concentration will be altered to maintain a target BIS of 50 during induction and maintenance of anesthesia
The target controlled infusion (TCI) pump will be programmed to Schneider model with the target effect site concentration of 3-µg/ml.
The effect-site concentration will be altered to maintain a target BIS of 50 during induction and maintenance of anesthesia
Manual propofol administration will be done using an intravenous infusion pump to maintain a target BIS of 50 during induction and maintenance of anesthesia.
|
|
Active Comparator: Manual group
Propofol administration will be controlled manually using an intravenous infusion pump to maintain a target BIS of 50 during induction and maintenance of anesthesia.
|
Propofol administration rate will be controlled by a feedback loop facilitated by BIS monitoring using the closed loop anaesthesia delivery system (CLADS).
A BIS value of 50 will be used as the target point for induction and maintenance of anaesthesia.
The target controlled infusion (TCI) pump will be programmed to marsh model with the target plasma site concentration of 3-µg/ml.
The plasma concentration will be altered to maintain a target BIS of 50 during induction and maintenance of anesthesia
The target controlled infusion (TCI) pump will be programmed to Schneider model with the target effect site concentration of 3-µg/ml.
The effect-site concentration will be altered to maintain a target BIS of 50 during induction and maintenance of anesthesia
Manual propofol administration will be done using an intravenous infusion pump to maintain a target BIS of 50 during induction and maintenance of anesthesia.
|
What is the study measuring?
Primary Outcome Measures
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Anaesthesia depth consistency
Time Frame: From end of surgery till 8 hours intraoperatively
|
It will be determined by the percentage of the anaesthesia time during which the BIS remained +/- 10 of the target BIS of 50
|
From end of surgery till 8 hours intraoperatively
|
Secondary Outcome Measures
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Intra-operative heart Rate (beats per minute)
Time Frame: From beginning of anaesthesia till 10 hours intraoperatively
|
Comparison of intra-operative heart rate between the study arms will be done
|
From beginning of anaesthesia till 10 hours intraoperatively
|
|
Intra-operative systolic , diastolic, and mean blood pressure (mmHg)
Time Frame: From beginning of anaesthesia till 10 hours intraoperatively
|
Comparison of intra-operative blood pressure- systolic, diastolic, and mean blood pressure between the study arms will be done
|
From beginning of anaesthesia till 10 hours intraoperatively
|
|
Postoperative sedation
Time Frame: From end of anaesthesia till 24-hours postoperatively
|
Will be assessed using Modified Observer's assessment of alertness/sedation scale.
The scale has a maximum value of '5', which refers to a fully awake patient and a minimum value of '0' which refers to a deeply sedated patient.
|
From end of anaesthesia till 24-hours postoperatively
|
|
Performance characteristic of propofol delivery system
Time Frame: From end of surgery till 10-hours intraoperatively
|
It will be determined using the Varvel criteria parameter :median performance error (MDPE).
This parameter is calculated by the computer software which analyses the intraoperative BIS data.
This parameter have no unit of measurement.
Its just a abstract number.
|
From end of surgery till 10-hours intraoperatively
|
|
Performance characteristic of propofol delivery system
Time Frame: From end of surgery till 10-hours intraoperatively
|
It will be determined using the Varvel criteria parameter: median absolute performance error (MDAPE).This parameter is calculated by the computer software which analyses the intraoperative BIS data.
This parameter have no unit of measurement.
Its just a abstract number.
|
From end of surgery till 10-hours intraoperatively
|
|
Performance characteristic of propofol delivery system
Time Frame: From end of surgery till 10-hours intraoperatively
|
It will be determined using the Varvel criteria parameter: wobble.
This parameter is calculated by the computer software which analyses the intraoperative BIS data.
This parameter have no unit of measurement.
Its just a abstract number..
|
From end of surgery till 10-hours intraoperatively
|
|
Performance characteristic of propofol delivery system
Time Frame: From end of surgery till 10-hours intraoperatively
|
It will be determined using the Varvel criteria parameter: global score.
It is calculated using the formula Median absolute performance error + wobble / percentage of the anesthesia time during which the BIS remained +/- 10 of the target BIS of 50.
This parameter have no unit of measurement.
Its just a abstract number..
|
From end of surgery till 10-hours intraoperatively
|
|
Propofol induction dose (mg/kg)
Time Frame: From start of propofol injection till 2-minutes intraoperatively
|
Dose of propofol required for induction of anaesthesia
|
From start of propofol injection till 2-minutes intraoperatively
|
|
Propofol maintenance dose (mg/kg/hr)
Time Frame: From 2-minutes intraoperatively till 10-hours intraoperatively
|
Dose of propofol required for maintenance of anaesthesia
|
From 2-minutes intraoperatively till 10-hours intraoperatively
|
|
Early recovery from anaesthesia
Time Frame: From end of anaesthesia till 20-minutes postoperatively
|
Time taken by the patient to open his/her eyes after discontinuation of anaesthesia will be noted
|
From end of anaesthesia till 20-minutes postoperatively
|
|
Early recovery from anaesthesia
Time Frame: From end of anaesthesia till 20-minutes postoperatively
|
Time taken for tracheal extubation after discontinuation of anaesthesia will be noted
|
From end of anaesthesia till 20-minutes postoperatively
|
|
Induction Time
Time Frame: From beginning of anesthesia till 5-minutes intraoperatively
|
Time taken for for induction of anesthesia i.e. time taken from starting propofol infusion till a target BIS value of 50 is achieved
|
From beginning of anesthesia till 5-minutes intraoperatively
|
Collaborators and Investigators
Sponsor
Sponsor
Investigators
Investigators
- Study Chair: Jayashree Sood, MBBS, MD, FFRCA, PGDHHM, FICA, Sir Ganga Ram Hospital, New Delhi, INDIA
- Study Director: Goverdhan D Puri, MBBS, MD, PhD, Postgraduate Institute for Medical Education & Research, Chandigarh, India
- Principal Investigator: Nitin Sethi, MBBS, DNB, Sir Ganga Ram Hospital, New Delhi, INDIA
- Principal Investigator: Amitabh Dutta, MBBS, MD, PGDHR, Sir Ganga Ram Hospital, New Delhi, INDIA
Study record dates
Study Major Dates
Study Start (Actual)
Study Start
Primary Completion (Actual)
Primary Completion
Study Completion (Actual)
Study Completion
Study Registration Dates
First Submitted
First Submitted
First Submitted That Met QC Criteria
First Submitted That Met QC Criteria
First Posted (Actual)
First Posted
Study Record Updates
Last Update Posted (Actual)
Last Update Posted
Last Update Submitted That Met QC Criteria
Last Update Submitted That Met QC Criteria
Last Verified
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
Other Study ID Numbers
- EC/12/20/1787
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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