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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01379352
Other study ID # 2011-04-015
Secondary ID
Status Completed
Phase N/A
First received June 21, 2011
Last updated December 24, 2013
Start date June 2011
Est. completion date December 2011

Study information

Verified date December 2013
Source Samsung Medical Center
Contact n/a
Is FDA regulated No
Health authority South Korea: Institutional Review Board
Study type Observational

Clinical Trial Summary

The vecuronium requirements may be reduced for recipients of living donor liver transplantation, as the vecuronium is eliminated principally by the liver. Furthermore, the requirements may be different according to the phase of surgery. The requirements may also be different according to the preoperative hepatic function as measured by MELD score during prehepatic phase, or graft to recipient body weight ratio (GRWR) during neohepatic phase. Therefore, the investigators are trying to investigate the difference of vecuronium requirements according to the phase of surgery or MELD score, GRWR.


Description:

The vecuronium requirements may be reduced for recipients of living donor liver transplantation, as the vecuronium is eliminated principally by the liver. Furthermore, the requirements may be different according to the phase of surgery. The requirements may by further reduced during anhepatic phase of liver transplantation. And the requirements may be increased as the graft functions during neohepatic phase.

We also postulated that the requirements may be different according to the preoperative hepatic function during preanhepatic phase, and according to the graft to recipient body weight ratio (GRWR) during neohepatic phase.

Therefore, we are trying to investigate the difference of vecuronium requirements according to the phase of surgery, MELD score, GRWR.


Recruitment information / eligibility

Status Completed
Enrollment 35
Est. completion date December 2011
Est. primary completion date December 2011
Accepts healthy volunteers No
Gender Both
Age group 20 Years to 69 Years
Eligibility Inclusion Criteria:

- patients undergoing elective living donor liver transplantation

Exclusion Criteria:

- patients who can not undergo train-of-four test due to central or peripheral neuromuscular disease.

- patients with severe cardiopulmonary diseases.

- patients who received transfusion with more than 10 units of packed red blood cells.

- primary non-functioning graft immediately after reperfusion of the graft.

- patients who administered drugs that influences the metabolism of vecuronium (such as anticonvulsant: phenytoin, carbamazepine, primidone, sodium valproate)

- patients undergoing cadaver donor liver transplantation

Study Design

Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
Korea, Republic of Samsung Medical Center Seoul

Sponsors (1)

Lead Sponsor Collaborator
Samsung Medical Center

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary vecuronium requirements during preanhepatic phase total vecuronium requirements as guided by Train-of-four neuromuscular monitoring during preanhepatic phase during prehepatic phase of liver transplantation No
Primary vecuronium requirements during anhepatic phase total vecuronium requirements as guided by Train-of-four neuromuscular monitoring during anhepatic phase during anhepatic phase of liver transplantation No
Primary vecuronium requirements during neohepatic phase total vecuronium requirements as guided by Train-of-four neuromuscular monitoring during neohepatic phase during neohepatic phase of liver transplantation No
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