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Clinical Trial ● Currently Recruiting NCT07806266

EORTC Metastatic Breast Cancer Module Development

EORTC Metastatic Breast Cancer Module Development — Recruiting • Oncology • NCT07806266.

📅 08 Sep 2026 ⏱ 2 min read
Currently Recruiting
This trial is actively seeking participants in the UK. Discuss eligibility with your patient before referring.
Status
Currently Recruiting
NCT ID
NCT07806266
Sponsor
University of Leeds
Start
2020-05-01
ClinicaliQ Trial Snapshot
  • EORTC Metastatic Breast Cancer Module Development — Recruiting • Oncology • NCT07806266.
  • Sponsor: University of Leeds.

Verify eligibility, endpoints and current status on the original source registry before acting on this summary.

Use This Page For
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  • Connecting this trial to nearby guidelines, Drug Science and education.
What This Trial Is Studying

The overall aim of this project is to help improve the Health Related Quality of Life (HRQOL) of metastatic breast cancer (MBC) patients. There is currently an urgent and unmet need for specific tools to aid in the evaluation of HRQOL in MBC and this project aims to address these needs by developing a comprehensive EORTC questionnaire for assessing the HRQOL of this group. The new module will be used in conjunction with EORTC QLQ-C30 and will provide better measurement of the quality of life issues experienced by women with…

Eligibility Snapshot
  • : * Adult females aged 18 years or over. * Have a diagnosis of MBC (Breast cancer that has spread to another part of the body), including de novo MBC patients. Patients with brain metastases will be included, providing there is no associated major cognitive impairment. * Have received (patients under observation) or currently receiving treatment for MBC, including chemotherapy, hormone therapy, targeted agents (anti-HER2, CDK4/6 inhibitors, mTOR/PIK3CA inhibitors, PARP inhibitors, immune therapy), radiotherapy and combinations. * Conversant in the language of questionnaire administration. * Have the capacity to give informed consent.

Use the source registry for the full inclusion and exclusion criteria before discussing referral or enrolment.

Full Trial Details
View this trial on the source registry
Eligibility criteria, protocol, and results when available
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