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Clinical Trials/ACTRN12620000198921
ACTRN12620000198921
Recruiting
Phase 3

SOOThe: Study of Obesity-reduction and Opiate-free Total Intravenous Anaesthesia (TIVA). Using TIVA in bariatric surgery improve the analgesia and reduce post operative nausea and vomiting.

Department of Anaesthesia0 sites130 target enrollmentFebruary 20, 2020

Overview

Phase
Phase 3
Intervention
Not specified
Conditions
Obesity
Sponsor
Department of Anaesthesia
Enrollment
130
Status
Recruiting
Last Updated
3 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
February 20, 2020
End Date
TBD
Last Updated
3 years ago
Study Type
Interventional
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Elective, cognisant, adult patients booked for elective gastric reduction surgery

Exclusion Criteria

  • \[1] Patients with a history of chronic pain
  • \[2] Patients with a history of dementia or cognitive impairment
  • \[3] Patients that do not wish to consent to the study
  • \[4] Patients with a history of significant allergy or anaphylaxis to Ketamine, Propofol, Opiates and lignocaine
  • \[5] Patients who are under 16 years of age or who are above 80 years of age
  • \[6] Patients who plan not to be an inpatient for 48 hours following surgery
  • \[7] Patients with a significant history of ischaemic heart disease (IHD) who have existing arrhythmias, low left or right ejection fraction (below 40%) or raised pulmonary blood pressure
  • \[8] Patients already prescribed sodium channel blockers as part of the management of pre\-existing IHD
  • \[9] Pregnancy

Outcomes

Primary Outcomes

Not specified

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