Selenium in the Prevention of Cancer

NCT01819649 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 491

Last updated 2017-09-14

No results posted yet for this study

Summary

This is a pilot study proceeding an intended international trial.

Hypothesis: Daily intake of selenium supplementation in the form of selenium-enriched yeast tablets will reduce the risk of cancer in healthy individuals.

Objective: The objective of this pilot study was to assess the viability of a full scale randomised trial.

AMENDMENT TO STUDY OBJECTIVE: Mortality analysis during intervention and follow-up as specified in the sections concerning study design and outcome measures.

Conditions

Interventions

DIETARY_SUPPLEMENT

SelenoPRECISE selenium-enriched yeast tablet, Pharma Nord Denmark A/S

Sponsors & Collaborators

  • Danish Cancer Society

    collaborator OTHER
  • University of Southern Denmark

    collaborator OTHER
  • K. A. Rohde's and wife's Foundation

    collaborator OTHER
  • The County of Funen, Denmark

    collaborator OTHER_GOV
  • Cypress Systems, USA

    collaborator UNKNOWN
  • The Dagmar Marshall Foundation

    collaborator OTHER
  • The N. O. Andersen Foundation

    collaborator UNKNOWN
  • The Danish Directory of Food and Agriculture

    collaborator UNKNOWN
  • The Foundation of Clinical Experimental Cancer Research, Odense

    collaborator UNKNOWN
  • The Foundation of Lily Benthine Lund

    collaborator UNKNOWN
  • The Memory Foundation of Merchant Brogaard

    collaborator UNKNOWN
  • Pharma Nord

    collaborator INDUSTRY
  • Odense University Hospital

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
60 Years
Max Age
74 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
1998-11-30
Primary Completion
2004-06-30
Completion
2004-06-30

Countries

  • Denmark

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01819649 on ClinicalTrials.gov