Clinical Trials Directory

Trials / Unknown

UnknownNCT03747094

Sedation of Morbidly Obese for Balloon Insertion

Fentanyl Versus Ketamine Supplementation for Prpofol Anesthesia During Balloon Insertion in Morbidly Obese Patients

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
70 (estimated)
Sponsor
Mansoura University · Academic / Other
Sex
All
Age
20 Years – 45 Years
Healthy volunteers
Not accepted

Summary

This prospective study will assess the value of different supplements to orpofol bases anesthesia in morbidly obes e patients scheduled for balloon insertion. Two common drugs will be added to propofol bases anesthesia;Ketamine or fentanyl. Effect on prpofol consumption, post-procedure recovery profile, and patient satisfaction will be the study objectives.

Conditions

Interventions

TypeNameDescription
DRUGFentanyl0.5 mic/kg fentanyl will be given immediately before the procedure
DRUGKetamine0.25 mg ketamine will be administered immediately before the procedure

Timeline

Start date
2018-12-01
Primary completion
2019-03-20
Completion
2019-04-15
First posted
2018-11-20
Last updated
2018-11-20

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT03747094. Inclusion in this directory is not an endorsement.