Clinical Trials Directory

Trials / Terminated

TerminatedNCT05031065

Prognostic Indicators for Radiation-induced Breast Fibrosis

Identifying Prognostic Indicators for the Development of Radiation-induced Breast Fibrosis

Status
Terminated
Phase
Study type
Observational
Enrollment
4 (actual)
Sponsor
AHS Cancer Control Alberta · Academic / Other
Sex
Female
Age
40 Years
Healthy volunteers
Not accepted

Summary

To study the inflammatory response during and after radiotherapy, especially by measuring the concentration of an enzyme called autotaxin and its product LPA in the blood plasma.

Detailed description

To study the inflammatory response during and after radiotherapy, especially by measuring the concentration of an enzyme called autotaxin and its product LPA in the blood plasma. Autotaxin and LPA cause fibrosis in other situation, but they have not been tested in radiation-induced fibrosis. We will determine if the duration and magnitude of the autotaxin and LPA responses are prognostic for the 15-28% of patients who will develop fibrosis. This fibrosis will be detected by ultrasound and a novel application of elastography, which should provide much earlier and quantifiable fibrotic changes compared to conventional physical examination.

Conditions

Interventions

TypeNameDescription
RADIATIONBreast Cancer Radiotherapy4000-4250 cGy in 15-16 daily fractions

Timeline

Start date
2024-01-24
Primary completion
2025-05-05
Completion
2025-05-05
First posted
2021-09-01
Last updated
2025-06-27

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT05031065. Inclusion in this directory is not an endorsement.

Prognostic Indicators for Radiation-induced Breast Fibrosis (NCT05031065) · Clinical Trials Directory