Evaluation of Propofol Dosing Based on Total Body Weight Using Closes-loop Anaesthesia Delivery System

Recruiting Phase 4 Interventional Study
Obesity, Morbid Anesthesia Propofol
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Prior Safety Data This treatment has already been tested in at least one earlier human trial.
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At a Glance
Age
18 – 65
Sex
Any
Trial phase
Phase 4
Study type
Interventional
Purpose
Basic Science
Participants needed
46 (estimated)
Sponsor
Sir Ganga Ram Hospital · Other
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About This Trial
The pharmacokinetic profile of various drugs is altered in obese patients especially those administered by the intravenous route. Propofol is the commonly used intravenous anesthetic agent for induction and maintenance of anaesthesia as part of total intravenous anaesthesia (TIVA) regimen. A major concern with propofol dosing based on total body weight (TBW) in obese patients is disproportionate d…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: 1. ASA physical status II/III 2. laparoscopic and non-laparoscopic surgery of more than 60-minutes duration 3. Body mass index \> 35kg/m2 Exclusion Criteria: 1. Cardiovascular disorders (uncontrolled hypertension, Atrio-ventricular block, sinus bradycardia, congenital heart di…
Contacts

Nitin Sethi, DNB

+919717494498

nitinsethi77@yahoo.co.in

CONTACT

Amitabh Dutta, MD, PGDHR

00919810873804

duttaamitabh@yahoo.co.in

CONTACT