TerminatedNot applicableNCT00681512
Official study title

The Effect of Berries on Lung Cancer Tumors

Study summary

The purpose of this study is to determine how berries affect cancer tumors in patients with non-small cell lung cancer.

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Key things to know

Main goalBasic Science

This describes the study’s primary purpose.

What is being studiedberry powder

The study team can explain what participation involves.

Who it may be forNon-small cell lung cancer (NSCLC)

These are broad labels—not an eligibility decision.

Checked against the public recordLast updated Feb 6, 2018 · Source: ClinicalTrials.gov

Is enrollment open?Terminated

Ask the study team to confirm whether enrollment is open.

What kind of study?Not applicable

Interventional

Where is it offered?1 U.S. location

Locations may change over time.

Who runs it?University of Louisville

Study sponsor

01
Study overview

What this study is about

Purpose
Basic Science
Study type
Interventional
Phase
Not applicable
Sponsor
University of Louisville
Interventions being studied
Dietary Supplement: berry powder
02
Explore related studies

How this study is categorized

These labels come from structured fields and exact terms in the public record.

03
Public criteria

Who may be able to participate

The sponsor separates these requirements into two groups. You do not need to interpret them alone—use them to guide a conversation with the study team.

Requirements people may need to meetInclusion criteria
  • (lung cancer survivors):
  • men treated for lung cancer, women treated for lung cancer and with no child-bearing potential (hysterectomy, tubal ligation, post-menopausal women)
Reasons someone may not be able to joinExclusion criteria
  • (lung cancer survivors):
  • women who are on hormone replacement therapy
  • women who are pregnant, or planning for pregnancy
  • history of lung transplant
  • prison inmate
  • inability to take oral medication or food
  • known or suspected allergy to berries or berry products
  • HIV patients Inclusion Criteria (volunteers):
  • adult men, adult women with no child bearing potential (hysterectomy, tubal ligation, post-menopausal women)

Important: This is the sponsor’s public criteria, not a determination of eligibility. The study team must review your individual situation.

04
Study sites

U.S. locations

  • James Graham Brown Cancer CenterLouisville, Kentucky

Source and freshness
Processed from ClinicalTrials.gov. Last public update: Feb 6, 2018. Always confirm current availability with the study team.

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