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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03352349
Other study ID # Terlipressinum PVP
Secondary ID
Status Recruiting
Phase Phase 2
First received November 18, 2017
Last updated November 21, 2017
Start date December 1, 2017
Est. completion date December 30, 2018

Study information

Verified date November 2017
Source Shanghai Zhongshan Hospital
Contact Hui-Chuan Sun, MD&PhD
Phone +86-021-64041990
Email sun.huichuan@zs-hospital.sh.cn
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

In this study, investigators aim to screen out the patients with portal hypertension by monitoring intraoperative PVP, and to decide the effect of Terlipressinum on the portal pressure after liver resection.


Description:

Liver resection is a common treatment for liver tumors. But the incidence of postoperative liver failure after hepatectomy is as high as 9-18.6%, which results in relatively high mortality rate . Portal hypertension is considered as a contraindication for hepatectomy according to the guidelines of the European Society of Hepatology and the American Society of Hepatology. Recent studies found that patients with portal hypertension were more likely to have persistent liver failure and shorter long-term survival after liver resection operation, compared to patients without portal hypertension.

Most of liver cancer patients in China have disease backgroud including chronic hepatitis and cirrhosis. Among liver cancer patients, of which function is Child A or B and have indication for liver resection, 25% of them have portal hypertension.


Recruitment information / eligibility

Status Recruiting
Enrollment 30
Est. completion date December 30, 2018
Est. primary completion date October 30, 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years to 75 Years
Eligibility Inclusion Criteria:

1. Patients who receives liver resection.

2. PVP is more than 12mmHg in 5 minutes after liver resection.

Exclusion Criteria:

1. Age: <18, >75;

2. Portal vein tumor thrombus is confirmed by preoperative assays;

3. Obstruction of biliary tract;

4. Active hepatitis;

5. Previous history of myocardial infarction;

6. Previous history of chronic kidney disease;

7. Severe arrhythmia;

8. Any other contraindications of the Terlipressinum.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Terlipressinum
If the PVP is over 12 mmHg after hepatectomy, 1mg of Terlipressinum was given to patients intravenously. If the portal vein pressure is decreased by 1 mmHg, then 2mg of Terlipressinum was continuously given every day in the next 4 days after liver resection.

Locations

Country Name City State
China Zhongshan Hospital Shanghai Shanghai

Sponsors (1)

Lead Sponsor Collaborator
Shanghai Zhongshan Hospital

Country where clinical trial is conducted

China, 

References & Publications (2)

Chen X, Zhai J, Cai X, Zhang Y, Wei L, Shi L, Wu D, Shen F, Lau WY, Wu M. Severity of portal hypertension and prediction of postoperative liver failure after liver resection in patients with Child-Pugh grade A cirrhosis. Br J Surg. 2012 Dec;99(12):1701-10. doi: 10.1002/bjs.8951. — View Citation

Rahbari NN, Garden OJ, Padbury R, Brooke-Smith M, Crawford M, Adam R, Koch M, Makuuchi M, Dematteo RP, Christophi C, Banting S, Usatoff V, Nagino M, Maddern G, Hugh TJ, Vauthey JN, Greig P, Rees M, Yokoyama Y, Fan ST, Nimura Y, Figueras J, Capussotti L, Büchler MW, Weitz J. Posthepatectomy liver failure: a definition and grading by the International Study Group of Liver Surgery (ISGLS). Surgery. 2011 May;149(5):713-24. doi: 10.1016/j.surg.2010.10.001. Epub 2011 Jan 14. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Change of Portal vein pressure The change of the portal vein pressure before and after the use of Terlipressinum. 8 months
Secondary Incidence of hepatic dysfunction after hepatectomy 8 months
Secondary Incidence of acute renal dysfunction after hepatectomy 8 months
Secondary Adverse effect of Terlipressurinum 8 months