Skip to main content
Clinical Trials/IRCT20201024049135N1
IRCT20201024049135N1
Recruiting
Phase 3

Comparison of two methods of calculating the dose of propofol for induction of general anesthesia according to either Ideal Body Weight(IBW) or Fat Free Mass(FFM), in morbid obese patient: parallel double - blinded clinical trial

Iran University of Medical Sciences0 sites40 target enrollmentTBD

Overview

Phase
Phase 3
Intervention
Not specified
Conditions
Morbid obese.
Sponsor
Iran University of Medical Sciences
Enrollment
40
Status
Recruiting
Last Updated
5 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
5 years ago
Study Type
Interventional
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Obesity BMI more than 35
  • Age 18\-59 years
  • ASA ll and lll
  • Undergoing for bariatric surgery

Exclusion Criteria

  • Difficult airway
  • The need for awake intubation
  • Severe systemic diseases
  • Impaired renal and hepatic function
  • History of allergies to the drugs studied
  • Behavioral disorders and the use of psychiatric drugs

Outcomes

Primary Outcomes

Not specified

Similar Trials