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Breast Cancer Female Clinical Trials

Reviewed by TrialFinderData Editorial Team · Updated

6 recruiting trials for Breast Cancer Female. Eligibility criteria explained in plain English.

TrialFinderData lists 6 Breast Cancer Female clinical trials drawn from ClinicalTrials.gov, all of which are currently recruiting participants.

Every phased trial in this set is Phase 2 (1 of the listed studies); the remaining records are observational or have no phase recorded on ClinicalTrials.gov.

Research is led by Maastricht University Medical Center (1), Federal University of Alagoas (1), The Leeds Teaching Hospitals NHS Trust (1), among the most active sponsors registered for these trials.

The most frequently studied intervention is EVEBRA device (device, 1 trial), followed by Physical exercise, Cognitive testing.

Important: This information is not medical advice. Talk to your doctor about whether a clinical trial is right for you.
6
Total Trials
6
Recruiting Now
0
Phase 3 Trials
6
Sponsors

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Recruiting Trials

Clinical trial data sourced from the ClinicalTrials.gov registry, maintained by the National Library of Medicine. Always consult your doctor before considering any clinical trial.

RECRUITINGNCT05003635

External Vacuum Expansion: Evaluation in Breast Reconstructive Surgery Evaluation in Breast Reconstructive Surgery

This multicentre randomized controlled trial aims to evaluate a new breast reconstruction technique- autologous fat transfer (AFT). Female patients with breast cancer schedule to...

Sponsor: Maastricht University Medical CenterEnrolling: 903 locations
RECRUITINGNCT06547853

Physical and Health Outcomes With ExeRcise in Cancer SURVIVORS

This study aims to evaluate the effect of a physical exercise intervention model on breast cancer survivors and their adherence. The sample will consist of 30 women with a primary...

Sponsor: Federal University of AlagoasEnrolling: 301 location
RECRUITINGNCT07116642

Comparing Patient Reported Outcomes and Clinical Outcomes Based on Different Scar Placement in Patients Undergoing...

This study is for patients with breast cancer and the objective is to compare patient reported outcome measures (PROMs) based on scar placement in patients undergoing standard...

Sponsor: The Leeds Teaching Hospitals NHS TrustEnrolling: 1001 location
RECRUITINGNCT03137095

Effects of Chemotherapy on Cognitive Function in Breast Cancer Patients & Non-Cancer Control Subjects With Optional...

Study is enrolling newly diagnosed breast cancer patients about to start chemotherapy and age-matched control participants. The investigator is trying to better understand the...

Sponsor: University of RochesterEnrolling: 1501 location
RECRUITINGPhase 2NCT06176261

DATO-BASE: DATOpotamab-deruxtecan for Breast Cancer Brain metAstaSEs

The purpose of this study is to test the safety and effectiveness of the study drug datopotamab deruxtecan in participants with metastatic breast cancer that has spread to the...

Sponsor: Sarah Sammons, MDEnrolling: 583 locations
RECRUITINGNCT07505797

ATUSA Ultrasound Diagnostic Imaging for Breast Lesions Evaluation (AUDIBLE)

AUDIBLE is a multi-site, clinical study conducted in the United States aimed at gathering data on 3D Automated Breast Ultrasound imaging using the iSono Health ATUSA system. The...

Sponsor: iSono Health, Inc.Enrolling: 8001 location

Frequently Asked Questions

There are currently 6 clinical trials for Breast Cancer Female, with 6 actively recruiting participants. These include trials across all phases from early-stage Phase 1 to late-stage Phase 3.

To join a clinical trial for Breast Cancer Female, review the eligibility criteria on the trial detail pages, then talk to your doctor about whether a trial is right for you. Your doctor can help you evaluate the potential benefits and risks.

Phase 3 trials are large-scale studies that test whether a treatment is effective and monitor side effects. There are 0 Phase 3 trials for Breast Cancer Female, representing treatments closest to potential FDA approval.

Clinical trials follow strict safety protocols overseen by Institutional Review Boards (IRBs) and the FDA. Participants are monitored closely and can withdraw at any time. Always discuss risks and benefits with your healthcare provider before enrolling.

Sources: ClinicalTrials.gov, FDA
Last updated:

Trial data sourced from the ClinicalTrials.gov API. This site does not provide medical advice, always talk to your doctor about clinical trial participation.