The Effect of Fish Oils on Human Hepatic Colorectal Metastases
NCT ID: NCT00942292
Last Updated: 2013-06-25
Study Results
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Basic Information
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COMPLETED
PHASE2
20 participants
INTERVENTIONAL
2007-05-31
2010-10-31
Brief Summary
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Detailed Description
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Recent research has described the beneficial effects of intravenous fish oils for surgical patients, such as reduced hospital stay, reduced re-operation rate and reduced requirements for intravenous antibiotics. These are in part due to the anti-inflammatory effects of fish oils.
There is evidence that fish oils are also effective against cancer, large population studies indicate that diets rich in omega-3 are associated with a lower incidence of cancer, and in vitro and animal studies demonstrate anti-tumour effects of fish oils
1. Fish oils inhibit the growth of different human cancer cell lines
2. They act specifically on tumour cells only and do not impair the function of normal cells
3. EPA and DHA inhibit the growth of human cancer cell lines and enhance apoptosis.
4. Fish oil induces apoptosis in human colorectal cancer cell lines in-vitro after 48hrs incubation
5. Fish oil has been shown to inhibit the proliferation activities, inhibit the invasive activities and increase the apoptosis of human pancreatic carcinoma cell lines in-vitro after only 48hrs of exposure
6. Fish oil has been shown to enhance colorectal adenocarcinoma cell lines sensitivity to radiotherapy
7. Fish oil has also been shown to reduce the incidence of liver metastases in experimentally induced ductal pancreatic cancer in rats after 30 weeks of oral treatment with an omega-3 supplemented diet.
8. Lung cancer xenografts in animals fed with fish oil showed significantly increased tumour regression in response to doxorubicin compared to those fed with omega-3.
This study aims to assess the effect of omega-3 FA upon hepatic colorectal metastases in a pilot study. 20 patients will be selected for this pilot study with potentially resectable hepatic colorectal adenocarcinoma metastases. 10 patients will receive total parenteral nutrition (TPN) without fish oils (controls), 10 will receive fish oil containing lipid emulsion in their TPN.
Changes in tumour angiogenesis (increased angiogenesis is associated with a poorer prognosis in hepatic colorectal metastases) will be investigated using digital contrast enhanced MRI scanning, and markers of angiogenesis will be investigated in blood and resected tumour samples from the patients.
It is a randomised controlled double blind trial.
Conditions
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Study Design
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RANDOMIZED
FACTORIAL
TREATMENT
TRIPLE
Study Groups
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Lipidem (fish oil)
Lipidem (TPN containing fish oil)
Lipidem- fish oil emulsion BBraun UK
Digital Contrast MRI scan
Lipofundin (TPN)
Control arm (no fish oil)
Lipidem- fish oil emulsion BBraun UK
Digital Contrast MRI scan
Interventions
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Lipidem- fish oil emulsion BBraun UK
Digital Contrast MRI scan
Eligibility Criteria
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Inclusion Criteria
2. Able to give informed written consent
3. Diagnosis of respectable hepatic colorectal metastases on radiological and laparoscopic appearances
Exclusion Criteria
2. Hypersensitivity to fish-, egg-, or soy protein, or to any of the active substances or constituents in the lipid emulsion
3. Hyperlipidaemia
4. Severe blood coagulation disorders
5. Severe renal insufficiency (Creatinine \>200)
6. Any general contra-indications to infusion therapy - pulmonary oedema, hyperhydration, decompensated cardiac insufficiency
7. Any unstable medical conditions - uncontrolled diabetes mellitus, acute myocardial infarction, stroke, embolic disease, metabolic acidosis, sepsis, pancreatitis
8. Patients undergoing conventional neo-adjuvant chemotherapy.
18 Years
80 Years
ALL
No
Sponsors
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B. Braun Melsungen AG
INDUSTRY
University Hospitals, Leicester
OTHER
Responsible Party
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Principal Investigators
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Ashley R Dennison, MBChB, FRCS, MD
Role: PRINCIPAL_INVESTIGATOR
Leicester General Hospital
Locations
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Leicester General Hospital
Leicester, Leicestershire, United Kingdom
Countries
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References
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Other Identifiers
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REC reference: 06/Q2501/160
Identifier Type: -
Identifier Source: secondary_id
EudraCT number: 2006-000044-71
Identifier Type: -
Identifier Source: secondary_id
10097
Identifier Type: -
Identifier Source: org_study_id
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