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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01457534
Other study ID # 4-2010-0671
Secondary ID
Status Completed
Phase N/A
First received October 4, 2011
Last updated February 26, 2013
Start date January 2011
Est. completion date February 2011

Study information

Verified date February 2013
Source Yonsei University
Contact n/a
Is FDA regulated No
Health authority Korea: Food and Drug Administration
Study type Observational

Clinical Trial Summary

Background. Acute renal failure after liver transplantation (LT) requiring continuous renal replacement therapy (CRRT) adversely affects patient survival. However, there are few reports to assess the predictors for postoperative CRRT in liver transplant patients. The investigators undertook this study to identify perioperative factors that would predict patients at risk of CRRT.

Patients and Methods. The investigators retrospectively reviewed the data of 148 liver transplant patients from January 2007 to November 2010 at Severance Hospital, Yonsei University HealthSystem, in Seoul, Korea. The number of patients treated with CRRT was 44 (18 patients from living and 26 from deceased donors) and those without CRRT was 104. Univariate and stepwise logistic multivariate analyses were performed.


Recruitment information / eligibility

Status Completed
Enrollment 148
Est. completion date February 2011
Est. primary completion date February 2011
Accepts healthy volunteers No
Gender Both
Age group 19 Years to 65 Years
Eligibility Inclusion Criteria:

- Age 19-65 year

- Liver transplant patients from January 2008 to December 2011

Exclusion Criteria:

- Patients treated with CRRT before transplantation

Study Design

Observational Model: Case Control, Time Perspective: Retrospective


Related Conditions & MeSH terms


Locations

Country Name City State
Korea, Republic of Severance Hospital Seoul

Sponsors (1)

Lead Sponsor Collaborator
Yonsei University

Country where clinical trial is conducted

Korea, Republic of, 

References & Publications (5)

Gonwa TA, Mai ML, Melton LB, Hays SR, Goldstein RM, Levy MF, Klintmalm GB. Renal replacement therapy and orthotopic liver transplantation: the role of continuous veno-venous hemodialysis. Transplantation. 2001 May 27;71(10):1424-8. — View Citation

Holt AW, Bierer P, Bersten AD, Bury LK, Vedig AE. Continuous renal replacement therapy in critically ill patients: monitoring circuit function. Anaesth Intensive Care. 1996 Aug;24(4):423-9. — View Citation

Matsubara S, Okabe K, Ouchi K, Miyazaki Y, Yajima Y, Suzuki H, Otsuki M, Matsuno S. Continuous removal of middle molecules by hemofiltration in patients with acute liver failure. Crit Care Med. 1990 Dec;18(12):1331-8. — View Citation

Wong LP, Blackley MP, Andreoni KA, Chin H, Falk RJ, Klemmer PJ. Survival of liver transplant candidates with acute renal failure receiving renal replacement therapy. Kidney Int. 2005 Jul;68(1):362-70. — View Citation

Wu CC, Yeung LK, Tsai WS, Tseng CF, Chu P, Huang TY, Lin YF, Lu KC. Incidence and factors predictive of acute renal failure in patients with advanced liver cirrhosis. Clin Nephrol. 2006 Jan;65(1):28-33. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary status before operation laboratory data(ex : total bilirubin, albumin, coagulation factors, blood gas analysis(arterial CO2 pressure. Blood urea nitrate/Creatinine, Hemoglobin/Hematocrit.) 1 day before operation No
Primary the amount of ascites intraoperative No
Primary the duration of anesthesia and operation intraoperative No
Primary intraoperative hemodynamic instability intraoperative No
Primary intraoperative bleeding intraoperative No
Primary Intraoperative urine output intraoperative No
Primary the types of donation(living or deceased donor) intraoperative No
Primary survival rate on the postoperative 28th days, 365 days No
Primary postoperative bleeding amount on the postoperative 28th days, 365 days. No
Primary postoperative CRRT(continuous renal replacement therapy), on the postoperative 28th days, 365days No
Primary mortality on the postoperative 28th days, 365 days. No
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