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Supplemental Selenium and Vitamin E and Pulmonary Function

The Respiratory Ancillary Study (RAS) to SELECT

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00063453
Enrollment
2920
Registered
2003-06-30
Start date
2003-08-31
Completion date
2010-08-31
Last updated
2017-12-12

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

Conditions

Chronic Obstructive Pulmonary Disease, Lung Diseases, Lung Diseases, Obstructive

Brief summary

To test whether supplementation with selenium and/or vitamin E affects pulmonary function.

Detailed description

BACKGROUND: There is compelling evidence from observational epidemiologic studies that intakes of nutrients with antioxidant properties are associated with reduced risks of chronic obstructive disease (COPD) and increased lung function. This study is ancillary to the multisite Selenium and Vitamin E Cancer Prevention Trial (SELECT), a 4-arm placebo-controlled, double-blinded randomized trial in 35,000 men testing whether daily supplementation with vitamin E (400mg alpha-tocopherol), selenium (200 micrograms selenomethionine) or both vitamin E and selenium can prevent prostate cancer. DESIGN NARRATIVE: This study is ancillary to the multisite Selenium and Vitamin E Cancer Prevention Trial (SELECT), a 4-arm placebo-controlled, double-blinded randomized trial in 35,000 men testing whether daily supplementation with vitamin E (400mg alpha-tocopherol), selenium (200 micrograms selenomethionine) or both vitamin E and selenium can prevent prostate cancer. A total of 3,000 SELECT participants will be enrolled for this respiratory ancillary study, and data collection will be extended to include pulmonary function, respiratory disease, and respiratory symptoms. Biological measures of nutrient exposure (serum vitamin E and selenium) and plasma lipids (total and high-density lipoprotein cholesterol) will be collected on all participants and oxidant burden (urinary F2-isoprostane) on a sub sample of heavy smokers and men with COPD. The primary outcome will be change over about 36 months in forced expiratory volume in the first second (FEV1). FEV1 is a valid and reliable measure of respiratory function that strongly predicts COPD and mortality. Extensive data on diet and dietary supplement use are being collected by the SELECT parent study. All specific aims examine pre-specified contrasts between the 4 arms of the SELECT randomized trial. The underlying hypothesis is that supplements will reduce the age related decline in FEV1 and thus at the 3-year follow-up FEV1, which will be tested in longitudinal and cross-sectional models. A secondary aim considers whether the effect of supplementation is greater among smokers (high burden of exogenous oxidants) who, by purposive selection of the study sites, will comprise about 25% of the sample.

Interventions

DIETARY_SUPPLEMENTVitamin E

vitamin E (400 IU/day all rac-α-tocopheryl acetate)

DIETARY_SUPPLEMENTSelenium

selenium (200 μg/d L-selenomethionine)

DIETARY_SUPPLEMENTVitamin E placebo

placebo

DIETARY_SUPPLEMENTSelenium placebo

placebo

Sponsors

National Heart, Lung, and Blood Institute (NHLBI)
CollaboratorNIH
Cornell University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
FACTORIAL
Primary purpose
PREVENTION
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
MALE
Age
50 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

Eligibility criteria: * age ≥ 55 y (≥ 50 y in African-Americans) * serum prostate-specific antigen ≤ 4ng/mL * no clinical evidence of prostate cancer

Exclusion criteria

* Off both SELECT supplements

Design outcomes

Primary

MeasureTime frame
Change in pulmonary function over time by arm of studyOutcome is assessed at annual and bi-annual study visits, during in-person visit of participant to the study site. Over a period of about 36 to 48 months, participants are assessed between 3 and 4 times

Other

MeasureTime frameDescription
Effect of selenium and vitamin E supplementation on incidence of COPDQuestionnaire data on incident lung disease is assessed at annual and biannual study visits, in all SELECT participants. These questionnaire data were collected through the end of SELECT active follow-up, which was December 2010The incidence of COPD will be assessed in the full SELECT trial, given this ancillary study added questionnaire data to assess self-reported incidence of lung disease in the full 35,000 participants

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 12, 2026