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Clinical Trials/NL-OMON48996
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

Radboud Universitair Medisch Centrum0 sites10 target enrollmentTBD

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.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional

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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