Actively Recruiting

Age: 18Years +
FEMALE
NCT04878666

Prospective Assessment of Quality of Life in Patients With Locally Recurrent Breast Cancer and Hyperthermic Radiotherapy

Led by University Hospital Tuebingen · Updated on 2021-05-07

20

Participants Needed

1

Research Sites

334 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Prospective assessment of Quality of Life in patients with locally recurrent breast cancer after close R0, R1 or R2 resection or local inoperability and hyperthermic radiotherapy.

CONDITIONS

Official Title

Prospective Assessment of Quality of Life in Patients With Locally Recurrent Breast Cancer and Hyperthermic Radiotherapy

Who Can Participate

Age: 18Years +
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Histologically confirmed local recurrence of breast cancer after close resection (≤1mm margin), R1 or R2 resection, or inoperable chest wall recurrence
  • Female patients aged 18 years or older
  • ECOG performance status of 0 to 2
  • Estimated life expectancy greater than 2 years
  • Provided informed consent
Not Eligible

You will not qualify if you...

  • Extensive distant metastases with an estimated life expectancy less than 2 years
  • Severe heart disease including NYHA III/IV heart failure, recent myocardial infarction within 6 months, coronary heart disease, or third-degree AV block
  • Presence of a cardiac pacemaker
  • Second malignancy except certain controlled cancers (cervical carcinoma in situ, local basaliomas, superficial bladder carcinomas Ta, Tis, T1) treated curatively more than 5 years ago
  • Pregnancy or breastfeeding
  • Implanted port on the side treated with hyperthermia (contralateral side ports allowed)
  • Subclavian vein thrombosis within the last 6 months
  • Other conditions preventing hyperthermia treatment
  • Conditions preventing regular follow-up care
  • Organ transplant recipients
  • Other implants on the ipsilateral chest wall

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

University Hospital Tübingen, Department of Radiation Oncology

Tübingen, Baden-Wurttemberg, Germany, 72076

Actively Recruiting

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Research Team

V

Vanessa Heinrich, MD

CONTACT

D

Daniel Zips, MD, Prof.

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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