Skip to main content
OpenTrials
Completed

NCT Number: NCT00432913

Effect of 2 Doses of EPA on Apoptosis and Cell Proliferation on Colon Mucosa

The purpose of this study is to determine the effect of two doses purified EPA (an omega-3 fatty acid), on apoptosis (natural cell death) and cell proliferation (formation of new cells) in the lining of the colon for patients with a history of colonic polyps.

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2 / Phase 3

Primary location

S. Orsola Hospital, Bologna, Italy

Loading trial locations.

About this study

Colorectal cancer is generally accepted to develop from changes within colonic adenomatous polyps. More than 90% of new large bowel cancers arise sporadically. The molecular events leading to the development of colorectal cancer from polyps are characterised by an imbalance in cell proliferation (formation of new cells) and apoptosis (natural cell death) from changes in the genes involved in normal colon cells.

Recent work at St George's Hospital Medical School, London, has shown significant beneficial effects on cell proliferation and apoptosis rates in the lining of the colon in subjects with a history of colonic adenomas using a highly purified, free-fatty acid form of eicosapentaenoic acid (EPA).

Comparator(s): 2g EPA per day for 6 months and 1g EPA per day for 6 months will be compared against placebo for 6 months.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Males or females aged over 18
  • Patients of child-bearing potential must demonstrate a negative pregnancy test at screening, and should use a reliable form of contraception during the trial and for 1 month afterwards, e.g:
  • Oral contraceptive + condom
  • Intra-uterine device (IUD)+ condom
  • Diaphragm with spermicide + condom
  • Male partners of women of child bearing potential should use a reliable form of contraception during the trial and for 1 month afterwards, e.g:
  • Oral contraceptive + condom
  • Intra-uterine device (IUD)+ condom
  • Diaphragm with spermicide + condom
  • Patients must have a known history of colorectal adenomata and be under clinical follow-up for these, or be found to have one or more of these at the time of colonoscopy
  • Patients must have provided written informed consent to participate

Exclusion criteria

  • Patients who are allergic to fish
  • Patients who have diabetes mellitus
  • Patients who are pregnant or breast-feeding
  • Patients taking aspirin or other non-steroidal anti-inflammatory drugs on a regular basis
  • Patients who have aspirin-sensitive asthma
  • Patients suffering from haemorrhagic disorders
  • Patients who are taking warfarin or other anticoagulants
  • Patients who have significant abnormalities on their screening blood tests
  • Patients taking lipid lowering medication
  • Patients with known inflammatory bowel disease (IBD), or previously unknown IBD until discovered at the time of their colonoscopy
  • Patients with gastrointestinal malabsorptive disease
  • Patients belonging to a known polyposis syndrome (e.g. FAP, HNPCC)
  • Patients with a previous colonic resection for colorectal cancer
  • Patients who are taking other fish-oil supplements (e.g. cod liver oil) who are unwilling to stop them for the duration of the study
  • Patients who are deemed mentally incompetent, or have a history of anorexia nervosa or bulimia
  • Patients with a history of alcohol or drug abuse, including laxative abuse
  • Patients considered by their physician unlikely to be able to comply with the protocol.
  • Patients who have taken part in an experimental drug study in the preceding 2 months.

Treatment and study plan

Eicosapentaenoic Acid (EPA)

Drug

Either 2 x 500mg EPA capsules in the morning and evening (2g per day EPA) or 1 x 500mg EPA and 1 x placebo in the morning and evening (1g per day EPA)

Other names: ALFA

endoscopy

Procedure

At baseline, month 3 and month 6.

Other names: Colonoscopy, Flexible sigmoidoscopy

Biopsies taken

Procedure

9 biopsies taken for measurement of apoptosis (3 biopsies), cell proliferation (3 biopsies) and fatty acid levels (3 biopsies) at baseline, month 3 and month 6.

Clinical chemistry

Procedure

Full blood count at baseline, month 3 and month 6.

Haematology

Procedure

Urea and electrolytes, liver function tests, clotting profile and CRP at baseline, month 3 and month 6.

Physical Examination

Procedure

Including cardio-respiratory and abdominal examination at baseline, month 3 and month 6.

vital signs

Procedure

Height, weight, heart rate, blood pressure and temperature at baseline, month 3 and month 6.

Urine pregnancy test

Procedure

For subjects of child-bearing potential, urine pregnancy test at baseline, month 3 and month 6.

Completion of patient diary card

Procedure

Subjects are requested to complete when study medication is taken and in any new or unusual symptoms are experienced on a daily basis for 6 months.

Primary outcomes

  1. To measure levels of apoptosis in the normal colonic mucosa in subjects with a history of colonic adenomas, before and after treatment with EPA 99%.

    Time frame: 3 months and 6 months

  2. To measure levels of cell proliferation in the normal colonic mucosa in subjects with a history of colonic adenomas, before and after treatment with EPA 99%.

    Time frame: 3 months and 6 months

Secondary outcomes

  1. To measure the tissue content of EPA in the colonic mucosa before, during and after treatment with EPA.

    Time frame: 3 months and 6 months

  2. To determine the safety and tolerability of EPA.

    Time frame: 3 months and 6 months

Sponsors and collaborators

Lead sponsor

S.L.A. Pharma AG

Industry

Registry information

Official study title

The Effect of Two Dose Levels of Eicosapentaenoic Acid (EPA) on Apoptosis and Cell Proliferation in the Colonic Mucosa of Patients With a History of Colonic Polyps.

Important dates

Study start
2006
Primary completion
2008
Study completion
2008
First posted
Feb 8, 2007
Registry last updated
Oct 17, 2008

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.