Effects of Eicosapentaenoic Acid on Subjects at High Risk for Colorectal Cancer

NACompletedINTERVENTIONAL
Enrollment

25

Participants

Timeline

Start Date

January 31, 2014

Primary Completion Date

August 31, 2015

Conditions
Ulcerative Colitis
Interventions
DIETARY_SUPPLEMENT

Eicosapentaenoic Acid

Twenty patients with long-standing ulcerative colitis undergoing the usual colonoscopic surveillance + biopsy sampling will be recruited. At entry six extra biopsy samples will be collected from the colon. We will also collect blood (for serum, plasma and red cells isolation), urine and stools. Subjects will then receive 2 g/day of Eicosapentaenoic Acid (ALFA ™, SLA Pharma AG, Switzerland) as a supplement for 90 days. At the end of the study each subject will undergo sigmoidoscopy for the collection of 6 biopsies. Blood, urine and stools will be obtained prior to the procedure.

Trial Locations (1)

40138

Azienda Ospedaliero Universitaria Policlinico Sant'Orsola Malpighi, Bologna

All Listed Sponsors
lead

IRCCS Azienda Ospedaliero-Universitaria di Bologna

OTHER

NCT02069561 - Effects of Eicosapentaenoic Acid on Subjects at High Risk for Colorectal Cancer | Biotech Hunter | Biotech Hunter