NL-OMON48996
Completed
Phase 4
MRI measurement of the effects of moderate versus deep neuromuscular blockade on the abdominal working space during laparoscopic surgery in a prospective cohort study. - RELAX-2 study
Overview
- Phase
- Phase 4
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- Radboud Universitair Medisch Centrum
- Enrollment
- 10
- Status
- Completed
- Last Updated
- 2 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •\- all adult patients (18 years or older) scheduled for laparoscopic donor nephrectomy
- •\- obtained informed consent
Exclusion Criteria
- •\* Unable to provide informed consent
- •\* known or suspect allergy to mivacurium, rocuronium or sugammadex
- •\* neuromuscular disease
- •\* indication for rapid sequence induction
- •\* Being unable to undergo MRI due to any reason (e.g. non MRI\-compatible implants, epilepsy)
- •\* Deficiency of vitamin K\-dependent clotting factors, coagulopathy or active use of coumarin derivates.
- •\* Peri\-operative use of fusidic acid or flucloxacilline
- •\* Severe renal impairment (creatinine clearance \<30ml/min)
- •\* BMI\> 30 kg/m2
- •\* ASA\-score \> 2
Outcomes
Primary Outcomes
Not specified
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