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Terminated Phase 2 Interventional Results available

St. John's Wort in Relieving Hot Flashes in Postmenopausal Women With Non-Metastatic Breast Cancer

ClinicalTrials.gov ID: NCT00110136

Public ClinicalTrials.gov record NCT00110136. 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 26, 2026, 4:12 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

A Phase II Study of St. John's Wort for the Treatment of Hot Flashes in Women With a History of Breast Cancer

Brief summary

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

RATIONALE: St. John's wort may help relieve hot flashes in women with breast cancer. PURPOSE: This phase II trial is studying how well St. John's wort works in relieving hot flashes in women with non-metastatic breast cancer.

Study identification

NCT ID
NCT00110136
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Enrollment
9 participants

Conditions and interventions

Interventions

Drug

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 16, 2006 (Actual)
Primary completion
Apr 1, 2008 (Actual)
Completion
Apr 1, 2008 (Actual)
Last update posted
Sep 29, 2021

2006 – 2008

United States locations

U.S. sites
19
U.S. states
11
U.S. cities
19
Facility City State ZIP Site status
Helen F. Graham Cancer Center at Christiana Hospital Newark Delaware 19713 —
MBCCOP - Howard University Cancer Center Washington D.C. District of Columbia 20060 —
University of Miami Sylvester Comprehensive Cancer Center - Miami Miami Florida 33136 —
CCOP - Central Illinois Decatur Illinois 62526 —
CCOP - Northern Indiana CR Consortium South Bend Indiana 46601 —
Feist-Weiller Cancer Center at Louisiana State University Health Sciences Shreveport Louisiana 71130-3932 —
CCOP - Michigan Cancer Research Consortium Ann Arbor Michigan 48106 —
CCOP - Beaumont Royal Oak Michigan 48073-6769 —
CCOP - Metro-Minnesota Saint Louis Park Minnesota 55416 —
Cancer Research for the Ozarks Springfield Missouri 65804 —
CCOP - St. Louis-Cape Girardeau St Louis Missouri 63141 —
Alamance Cancer Center at Alamance Regional Medical Center Burlington North Carolina 27216 —
Hugh Chatham Memorial Hospital Elkin North Carolina 28621 —
CCOP - Southeast Cancer Control Consortium Goldsboro North Carolina 27534-9479 —
Leo W. Jenkins Cancer Center at ECU Medical School Greenville North Carolina 27835-6028 —
Wake Forest University Comprehensive Cancer Center Winston-Salem North Carolina 27157-1096 —
CCOP - Greenville Greenville South Carolina 29615 —
South Carolina Cancer Specialists Hilton Head Island South Carolina 29925 —
CCOP - Upstate Carolina Spartanburg South Carolina 29303 —

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 NCT00110136, 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 Sep 29, 2021 · Synced Oct 26, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00110136 live on ClinicalTrials.gov.

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