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Effect of a Perioperative Oral Nutritional Supplementation on Patients Undergoing Hepatic Surgery for Liver Cancer (IMPACT)

Primary Purpose

Liver Cancer, Hepatocellular Carcinoma, Cirrhosis

Status
Terminated
Phase
Phase 2
Locations
France
Study Type
Interventional
Intervention
Oral Impact®
Placebo
Sponsored by
Rennes University Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Liver Cancer focused on measuring Surgery, Liver Cancer, Cirrhosis, Nutrition

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Adult over 18 years Hepatectomy of at least 2 segments For primary or secondary cancer With cirrhosis (Child Pugh <8) or liver fibrosis (fibrosis score of 3) Informed written consent Exclusion Criteria: Pregnancy Recent weight loss of more than 10% of body weight Immunological deficiency Portal or hepatic arterial thrombosis Biliary duct dilation

Sites / Locations

  • Service de Réanimation Chirurgicale - Hôpital Pontchaillou

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

1

2

Arm Description

Perioperative Oral Nutritional Supplementation

Placebo of Perioperative Oral Nutritional Supplementation

Outcomes

Primary Outcome Measures

Factor V at day 3 after surgery

Secondary Outcome Measures

Liver regeneration kinetics (bile production at days 1, 3, 5 and 7;factor V, γ-glutathione transferase, α-foetoprotein at days 1, 3, 5, 7, 10 and 30; liver volume at days 10 and 30
Immunological biomarkers
Infections

Full Information

First Posted
September 8, 2005
Last Updated
February 24, 2012
Sponsor
Rennes University Hospital
Collaborators
Ministry of Health, France, Novartis
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1. Study Identification

Unique Protocol Identification Number
NCT00151671
Brief Title
Effect of a Perioperative Oral Nutritional Supplementation on Patients Undergoing Hepatic Surgery for Liver Cancer
Acronym
IMPACT
Official Title
Prospective, Randomized, Double Blind, Placebo-Controlled Study Evaluating the Effect of Oral Immune-Enhancing Nutritional Supplement on Hepatic Function After Liver Resection for Primary or Secondary Cancer on Cirrhosis or Liver Fibrosis
Study Type
Interventional

2. Study Status

Record Verification Date
September 2008
Overall Recruitment Status
Terminated
Why Stopped
insufficient enrollment rate
Study Start Date
April 2003 (undefined)
Primary Completion Date
April 2008 (Actual)
Study Completion Date
September 2008 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Rennes University Hospital
Collaborators
Ministry of Health, France, Novartis

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Cirrhotic patients undergoing hepatic resection have a mortality rate near 10%, and 30 to 70% of them develop severe complications. These failures are mainly due to hepatic insufficiency. Studies have already shown benefits of oral nutritional supplements in ORL, digestive, and cardiac surgery. We aimed to ascertain whether this nutritional, immune-enhancing supplementation, administered 7 days before and 3 days after surgery, could improve liver function and postoperative host defences in patients with liver cancer resection.
Detailed Description
In patients undergoing hepatic resection for liver cancer (with cirrhosis or fibrosis liver), mortality rate can reach 10% and morbidity (ascites, icteria, infections) 70%. These complications are mainly due to hepatic insufficiency: surgery leaves a reduced parenchyma, with oxidative stress lesions due to reperfusion injury. A good preoperative nutritional state has been shown to reduce complications and mortality. This can be amplified by preoperative nutrition with supplements containing L-arginin, ω3 polyunsaturated fatty acids, and nucleotides which boost immune responses, resistance to infections and liver function recovery. In this context, the study randomly assigns 50 patients who were scheduled to undergo hepatic resection, to receive either an oral immune-enhancing nutritional supplement or a placebo, for the 7 last preoperative and the first 3 postoperative days. The aim of the study is to evaluate the effects of this supplementation on liver function, immunity, and incidence of infections after surgery.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Liver Cancer, Hepatocellular Carcinoma, Cirrhosis, Liver Fibrosis
Keywords
Surgery, Liver Cancer, Cirrhosis, Nutrition

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 2, Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
35 (Actual)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Experimental
Arm Description
Perioperative Oral Nutritional Supplementation
Arm Title
2
Arm Type
Placebo Comparator
Arm Description
Placebo of Perioperative Oral Nutritional Supplementation
Intervention Type
Drug
Intervention Name(s)
Oral Impact®
Intervention Description
Oral nutritional supplement containing L-arginin, ω3 polyunsaturated fatty acids, and nucleotides. Given three times a day for the 7 last preoperative and the first 3 postoperative days.
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
Oral solution of placebo. Given three times a day for the 7 last preoperative and the first 3 postoperative days.
Primary Outcome Measure Information:
Title
Factor V at day 3 after surgery
Time Frame
day 3
Secondary Outcome Measure Information:
Title
Liver regeneration kinetics (bile production at days 1, 3, 5 and 7;factor V, γ-glutathione transferase, α-foetoprotein at days 1, 3, 5, 7, 10 and 30; liver volume at days 10 and 30
Time Frame
days 1, 3, 5, 7, 10 and 30
Title
Immunological biomarkers
Time Frame
Within 30 days
Title
Infections
Time Frame
Within 30 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Adult over 18 years Hepatectomy of at least 2 segments For primary or secondary cancer With cirrhosis (Child Pugh <8) or liver fibrosis (fibrosis score of 3) Informed written consent Exclusion Criteria: Pregnancy Recent weight loss of more than 10% of body weight Immunological deficiency Portal or hepatic arterial thrombosis Biliary duct dilation
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Yannick Mallédant, MD
Organizational Affiliation
Rennes University Hospital
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Eric Bellissant, MD, PhD
Organizational Affiliation
Rennes University Hospital
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Philippe Seguin, MD
Organizational Affiliation
Rennes University Hospital
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Karim Boudjema, MD, PhD
Organizational Affiliation
Rennes University Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Service de Réanimation Chirurgicale - Hôpital Pontchaillou
City
Rennes
ZIP/Postal Code
35033
Country
France

12. IPD Sharing Statement

Citations:
PubMed Identifier
11551575
Citation
Tepaske R, Velthuis H, Oudemans-van Straaten HM, Heisterkamp SH, van Deventer SJ, Ince C, Eysman L, Kesecioglu J. Effect of preoperative oral immune-enhancing nutritional supplement on patients at high risk of infection after cardiac surgery: a randomised placebo-controlled trial. Lancet. 2001 Sep 1;358(9283):696-701. doi: 10.1016/s0140-6736(01)05836-6.
Results Reference
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PubMed Identifier
10593328
Citation
Senkal M, Zumtobel V, Bauer KH, Marpe B, Wolfram G, Frei A, Eickhoff U, Kemen M. Outcome and cost-effectiveness of perioperative enteral immunonutrition in patients undergoing elective upper gastrointestinal tract surgery: a prospective randomized study. Arch Surg. 1999 Dec;134(12):1309-16. doi: 10.1001/archsurg.134.12.1309.
Results Reference
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PubMed Identifier
10199318
Citation
Braga M, Gianotti L, Radaelli G, Vignali A, Mari G, Gentilini O, Di Carlo V. Perioperative immunonutrition in patients undergoing cancer surgery: results of a randomized double-blind phase 3 trial. Arch Surg. 1999 Apr;134(4):428-33. doi: 10.1001/archsurg.134.4.428.
Results Reference
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Effect of a Perioperative Oral Nutritional Supplementation on Patients Undergoing Hepatic Surgery for Liver Cancer

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