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Not listed Phase 3 Interventional

Study for Treatment of Moderate or Severe, Periodic, "Cyclic", Breast Pain

ClinicalTrials.gov ID: NCT00237523

Public ClinicalTrials.gov record NCT00237523. 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 25, 2026, 1:27 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 III, Multicenter, Randomized, Double-Blind, Placebo-Controlled Study of IoGen™ for the Treatment of Moderate or Severe, Periodic Breast Pain Associated With Symptomatic Fibrocystic Breast Disease

Brief summary

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

* History of clinical breast pain for at least the last six months. * At least six days of moderate or severe breast pain per cycle. * Fibrosis, cysts, nodules involving at least 25% of the surface of one breast. * Euthyroid with no prior history of thyroid disease. * Six months of daily therapy with molecular iodine. * Placebo controlled vs active (1:1).

Study identification

NCT ID
NCT00237523
Recruitment status
Not listed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Symbollon Pharmaceuticals
Industry
Enrollment
175 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 50 Years
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
Jul 2005 (Type not available)
Primary completion
Not listed
Completion
Mar 2008 (Estimated)
Last update posted
Jun 18, 2007

2005 – 2008

United States locations

U.S. sites
39
U.S. states
24
U.S. cities
38
Facility City State ZIP Site status
Medical Affiliated Research Center, Inc. Huntsville Alabama 35801 —
Women's Health Research Phoenix Arizona 85015 —
Visions Clinical Research Tucson Arizona 85712 —
Expresscare Clinical Research Colorado Springs Colorado 80909-1691 —
Downtown Women's Heath Care Denver Colorado 80218 —
University of Colorado Denver Colorado 80262 —
S.H.E. Medical Associates Hartford Connecticut 06105 —
The GYN's Center for Women's Health Waterbury Connecticut 06708 —
Greater Hartford Women's Health Associates West Hartford Connecticut 06117 —
Visions Clinical Research Boynton Beach Florida 33437 —
Women's Medical Research Group, LLC Clearwater Florida 33759 —
Miami Research Associates, Inc. Miami Florida 33143 —
Palm Beach Research Center West Palm Beach Florida 33409 —
Soapstone Center for Clinical Research Decatur Georgia 30034 —
Fellows Research Alliance, Inc. Savannah Georgia 31406 —
Women's Health Practice Champaign Illinois 61820 —
Physicians Research Group Indianapolis Indiana 46250 —
University of Iowa Iowa City Iowa 52242 —
Kentucky Medical Research Center Lexington Kentucky 40504 —
York Clinical Consulting Marrero Louisiana 70072 —
MedVadis Research Wellesley Massachusetts 02481 —
Fallon Clinic Worcester Massachusetts 01608 —
University of Missouri Kansas City Missouri 64108 —
Department of Ob/Gyn - Women's Health University of Saint Louis St Louis Missouri 63117 —
The Medical Group of Northern Nevada Reno Nevada 89502 —
Women's Health Research Center, LLC Lawrenceville New Jersey 08648 —
Laurel Creek Research Associates Moorestown New Jersey 08057 —
Montefiore Medical Center/Albert Einstein College of Medicine The Bronx New York 10461 —
Wake Research Associates, LLC Raleigh North Carolina 27612 —
Radiant Research Cincinnati Ohio 45249 —
HWC Women's Research Center Miamisburg Ohio 45342 —
LION Research Norman Oklahoma 73071 —
Oregon Health & Science University Portland Oregon 97239 —
Penn State The Milton S. Hershey Medical Center Hershey Pennsylvania 17033 —
Drexel University College of Medicine Philadelphia Pennsylvania 19102-1192 —
Memorial Hospital of Rhode Island Pawtucket Rhode Island 02860 —
Fellows Research Alliance, Inc. Hilton Head Island South Carolina 29926 —
Women's Clinical Research Center/North Seattle Women's Group Seattle Washington 98105 —
Tacoma Women's Specialists Tacoma Washington 98405 —

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 NCT00237523, 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 Jun 18, 2007 · Synced Oct 25, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00237523 live on ClinicalTrials.gov.

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