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Completed Phase 2 Interventional

Soy Protein Supplement In Treating Hot Flashes in Postmenopausal Women Receiving Tamoxifen for Breast Disease

ClinicalTrials.gov ID: NCT00031720

Public ClinicalTrials.gov record NCT00031720. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 21, 2026, 5:10 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Phase II Study of Soy Protein to Treat Vasomotor Symptoms in Postmenopausal Women Taking Tamoxifen

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

RATIONALE: Soy protein supplement may be effective in reducing hot flushes in postmenopausal women who are receiving tamoxifen for breast disease. PURPOSE: Randomized phase II trial to determine the effectiveness of soy protein supplement in reducing hot flushes in postmenopausal women who are receiving tamoxifen for breast disease such as ductal hyperplasia or breast cancer.

Study identification

NCT ID
NCT00031720
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Enrollment
112 participants

Conditions and interventions

Interventions

Dietary Supplement · Drug · Other

Eligibility (public fields only)

Age range
18 Years and older
Sex
Female
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Mar 2002 (Type not available)
Primary completion
Apr 2006 (Actual)
Completion
Nov 2013 (Actual)
Last update posted
Jul 13, 2016

2002 – 2013

United States locations

U.S. sites
14
U.S. states
6
U.S. cities
12
Facility City State ZIP Site status
Center for Cancer Care at OSF Saint Anthony Medical Center Rockford Illinois 61108 —
Elkhart General Hospital Elkhart Indiana 46515 —
Howard Community Hospital Kokomo Indiana 46904 —
Center for Cancer Therapy at LaPorte Hospital and Health Services La Porte Indiana 46350 —
CCOP - Northern Indiana CR Consortium South Bend Indiana 46601 —
Memorial Hospital of South Bend South Bend Indiana 46601 —
Saint Joseph Regional Medical Center South Bend Indiana 46617 —
Commonwealth Hematology-Oncology, PC - Worcester Worcester Massachusetts 01605 —
Lakeland Regional Cancer Care Center - St. Joseph Saint Joseph Michigan 49085 —
Kingsbury Center for Cancer Care at Cheshire Medical Center Keene New Hampshire 03431 —
Norris Cotton Cancer Center at Dartmouth-Hitchcock Medical Center Lebanon New Hampshire 03756-0002 —
Wayne Memorial Hospital, Incorporated Goldsboro North Carolina 27534 —
Kinston Medical Specialists Kinston North Carolina 28501 —
FirstHealth Moore Regional Community Hospital Comprehensive Cancer Center Pinehurst North Carolina 28374 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00031720, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jul 13, 2016 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00031720 live on ClinicalTrials.gov.

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