Patient Guide: Endocrine Therapy-Induced Alopecia in Postmenopausal and Premenopausal Female Breast Cancer Patients

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 23 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT05612100
Status: 🟢 Enrolling Now
Condition: Breast Carcinoma
Phase: Not Specified

Where You Can Participate

This study is available at 23 locations across the country.

Top locations include:
  • • Albert Lea, Minnesota
  • • Baxter, Minnesota
  • • Bemidji, Minnesota
  • • And 20 more locations

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Endocrine Therapy-Induced Alopecia in Postmenopausal and Premenopausal Female Breast Cancer Patients - Join Clinical Trial NCTNCT05612100

How to Join This Clinical Trial - NCTNCT05612100

Learn how to participate in this Not Specified trial studying an investigational therapy for Breast Carcinoma. This study is currently enrolling participants.

Am I Eligible for This Clinical Trial?

This clinical research study is looking for participants with Breast Carcinoma. Eligibility requirements include specific age ranges, health status, and medical history. Contact the study team to learn if you qualify.

Condition Being Studied
Breast Carcinoma
Treatment Being Tested
Investigational treatment
Study Phase
Not Specified - Research study
Enrollment Status
Currently enrolling participants
Study Identifier
NCTNCT05612100 - ClinicalTrials.gov Identifier
Sponsored By
Study sponsor

What to Expect as a Participant

Participating in this clinical trial involves:

  • Initial screening to determine eligibility
  • Regular study visits and health assessments
  • Receiving the study treatment or placebo
  • Medical monitoring and follow-up care
  • Contributing to medical research that may help others
  • Potential access to new treatments before they're widely available

Clinical Trial Benefits and Compensation

Participants in this clinical research study may receive:

  • Close medical monitoring by healthcare professionals
  • Access to potential new treatments
  • Compensation for time and travel (varies by study)
  • No-cost study-related medical care
  • The opportunity to help advance medical knowledge

Where Is This Clinical Trial Located?

This study is enrolling participants at 23 locations. Find a study site near you:

Clinical Research Site

Albert Lea, Minnesota 56007 - United States

Status: RECRUITING

Clinical Research Site

Baxter, Minnesota 56425 - United States

Status: RECRUITING

Clinical Research Site

Bemidji, Minnesota 56601 - United States

Status: RECRUITING

Clinical Research Site

Brainerd, Minnesota 56401 - United States

Status: RECRUITING

Clinical Research Site

Deer River, Minnesota 56636 - United States

Status: RECRUITING

Clinical Research Site

Detroit Lakes, Minnesota 56501 - United States

Status: RECRUITING

Clinical Research Site

Duluth, Minnesota 55805 - United States

Status: RECRUITING

Clinical Research Site

Ely, Minnesota 55731 - United States

Status: RECRUITING

Clinical Research Site

Fosston, Minnesota 56542 - United States

Status: RECRUITING

Clinical Research Site

Grand Rapids, Minnesota 55744 - United States

Status: RECRUITING

And 13 more locations available. Contact us to find the nearest participating site.

How to Enroll in This Study

To learn more about participating in this Not Specified clinical trial for Breast Carcinoma:

  1. Review the eligibility criteria with your healthcare provider
  2. Contact the study team for a pre-screening interview
  3. Schedule an in-person screening visit if eligible
  4. Review and sign the informed consent form
  5. Begin participation in the clinical trial

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