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The Effect of Berries on Lung Cancer Tumors

Berry Interventional Trial (BIT) in Resected Non-Small Cell Lung Cancer

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00681512
Enrollment
6
Registered
2008-05-21
Start date
2008-04-30
Completion date
2013-12-31
Last updated
2018-02-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Non Small Cell Lung Cancer

Keywords

NSCLC, lung cancer, non small cell lung cancer, lung carcinoma

Brief summary

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

Detailed description

In the United States, more people (161,840 per year) die of lung cancers than of prostate cancer, breast cancer and colon cancer combined. Presently, there are over 43 million current smokers and over 47 million ex-smokers living in the US. Due to the lag time between smoking and the development of cancer, there are significant numbers of ex-smokers and current smokers who may develop lung cancer compared to never smokers. Recent studies in animals have shown that berries, given as a dietary supplement, are highly effective against certain types of cancers. In a study involving mice with lung tumors, mice that had consumed a mixture of berries developed fewer tumors and had less tumor growth than mice that did not consume berries. The berries used in this study will consist of blueberries, black raspberries, or a mixture of both.

Interventions

DIETARY_SUPPLEMENTberry powder

All subjects (lung cancer survivors and volunteers) will consume 20 grams of berry powder (blueberries, black raspberries, or a mixture of both) per day by mouth for the first 3 days, then 40 grams of berry powder by mouth every day for 4 to 5 weeks. The berry powder is to be mixed in subject's routine intake of milk, yogurt, juice, or water. All subjects will have the option to continue the berry regimen for an extended period. Subjects who choose to do so will not consume any berry powder for one week. After one week, subjects will begin consuming 40 grams of the berry powder every day for an additional 4 to 5 weeks.

Sponsors

James Graham Brown Cancer Center
CollaboratorOTHER
University of Louisville
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
BASIC_SCIENCE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion 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)

Exclusion 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)

Design outcomes

Primary

MeasureTime frameDescription
Assessment of blueberry and black raspberry phenolics in plasma and urineupon completion of 4 to 5 weeks of daily consumption of berry powderIn addition to determining the berry phytochemical profile in plasma and urine, this study will attempt to establish the effect of berries on modulating immunological profiles such as the complete blood count, and T, B and natural killer (NK) cell populations and circulating biomarkers (serum proteins and microRNAs). This pilot study will establish the safety and feasibility of conducting a larger clinical trial with berry intervention.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026