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Acute Pharmacokinetic-pharmacodynamic Change of Rocuronium After Reperfusion of Renal Graft

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Seoul National University

Status

Enrolling

Conditions

End Stage Renal Disease
Transplantation

Treatments

Drug: Rocuronium bromide

Study type

Interventional

Funder types

Other

Identifiers

NCT02827435
Roc_KTPL_PKPD

Details and patient eligibility

About

Reperfusion of renal graft in kidney transplantation can change the pharmacokinetic-pharmacodynamic (PKPD) parameters of rocuronium. The immediate increase of urine output during surgery may change the PKPD parameters of the drugs, including elimination rate. The goal of this study is to characterize the PKPD model of rocuronium during kidney transplantation and establish a basis for adequate dosage of rocuronium in kidney transplantation.

Through PKPD modeling, the changes during reperfusion of the renal graft will be evaluated. Furthermore, the factors related to the changes will be assessed. Adjusting the infusion rate according to the step of kidney transplantation will lead to stable muscle relaxation and fast recovery.

Enrollment

12 estimated patients

Sex

All

Ages

18 to 60 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • patients scheduled for elective living donor kidney transplantation
  • end stage renal disease with oliguria or anuria
  • normal BMI (BMI 18.5 ~ 25)
  • obtained informed consent

Exclusion criteria

  • patient with underlying neuromuscular disease

Trial design

Primary purpose

Basic Science

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

12 participants in 1 patient group

Rocuronium bolus
Experimental group
Description:
rocuronium bromide 1st bolus 0.1mg/kg, rocuronium bromide 2nd bolus 0.4mg/kg
Treatment:
Drug: Rocuronium bromide

Trial contacts and locations

1

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Central trial contact

Chul-Woo Jung, MD. PhD; Eun-Jin Chung, MD

Data sourced from clinicaltrials.gov

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