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NCT00597532 · ClinicalTrials.gov registry record · NA

Effect of Soy Supplementation on Cellular Markers in Normal and Cancerous Breast Tissue: A Randomized Placebo Controlled Study

A NA study, sponsored by Memorial Sloan Kettering Cancer Center.

Completed
Registry status
NA
Development phase
140
Enrollment target

NCT00597532: Completed NA study, sponsored by Memorial Sloan Kettering Cancer Center.

NCT00597532 is a NA study that has completed, run by Memorial Sloan Kettering Cancer Center. The registered enrollment target is 140 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (90% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

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The verdict

NCT00597532, a NA study, has completed, sponsored by Memorial Sloan Kettering Cancer Center.

COMPLETED
Registry status
NA
Development phase
140 participants
Enrollment target

Study Summary

To Test Effect of Soy Supplementation on Cellular Markers in Normal and Cancerous Breast Tissue using a Randomized Placebo Controlled Study. Objectives: * To determine (by immunohistochemistry) whether specific cellular markers and gene products associated with breast carcinoma can be altered by soy therapy. * To identify genes that can be altered by soy therapy in normal and neoplastic breast tissues by unbiased gene expression analysis using microarrays. * To compare specific cellular markers and pathways (immunohistochemistry), and gene expression using microarrays in normal and cancerous breast tissue.

Interventions

  • DIETARY_SUPPLEMENT Soy
  • DIETARY_SUPPLEMENT Milk

Trial Details

FieldValue
Enrollment Target 140 participants
Start Date 2002-08
Est. Completion 2016-04
Phase NA
Memorial Sloan Kettering Cancer Center

1,884 total trials

What the finished NCT00597532 record still lists

NCT00597532 is an interventional study that assigns participants to a tested intervention. The registered 140 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (90% lower).

The record links to 0 conditions, and to 2 interventions - of which Soy is the first listed.

NCT00597532 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00597532 about?

NCT00597532 is a clinical study titled "Effect of Soy Supplementation on Cellular Markers in Normal and Cancerous Breast Tissue: A Randomized Placebo Controlled Study". To Test Effect of Soy Supplementation on Cellular Markers in Normal and Cancerous Breast Tissue using a Randomized Placebo Controlled Study. Objectives: * To determine (by immunohistochemistry) whether specific cellular markers and gene products associated with breast carcinoma can be altered by s...

What is the current status of trial NCT00597532?

This trial is currently completed. It is a NA study. The enrollment target is 140 participants. The study started on 2002-08. Estimated completion is 2016-04.

What interventions are being tested in trial NCT00597532?

The interventions under investigation include: Soy (DIETARY_SUPPLEMENT), Milk (DIETARY_SUPPLEMENT).

Who is sponsoring clinical trial NCT00597532?

This trial is sponsored by Memorial Sloan Kettering Cancer Center, which has 1,884 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00597532's enrollment target sits among peer trials

140 713th of 2000 higher than 1,281 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT00597532, the US trial registry maintained by the National Library of Medicine. NCT00597532 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.