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RECRUITING
NCT04583254
PHASE2

Hypofractionated External-beam RadiOtherapy for Intact Cervical Cancer (HEROICC-Trial): A Feasibility Study

Sponsor: London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's

View on ClinicalTrials.gov

Summary

External radiation given in 25 fractions or so together with weekly chemotherapy and followed by 3 or 4 fractions of brachytherapy is the standard of care for patients with locally advanced cervical cancer. This study investigates the role of shortened external radiotherapy regimen (hypofractionated radiotherapy) by randomizing patients to this experimental regimen versus the standard of care.The purpose of this study is to access the feasibility of patient accrual to this trial in the Canadian setting and to provide an initial evaluation of cancer response and treatment tolerability.

Key Details

Gender

FEMALE

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

48

Start Date

2021-02-04

Completion Date

2028-12-14

Last Updated

2023-05-10

Healthy Volunteers

No

Conditions

Interventions

RADIATION

External beam radiotherapy (EBRT) + High-dose rate (HDR) Brachytherapy Experimental

40 Gy / 15 Fractions EBRT + HDR-Brachytherapy

RADIATION

External beam radiotherapy (EBRT) + High-dose rate (HDR) Brachytherapy Standard of Care

45 Gy / 25 Fractions EBRT + HDR-Brachytherapy

DRUG

Concurrent Chemotherapy

Weekly cisplatin 40 mg/m2 for a maximum of 5 cycles

Locations (3)

BC Cancer - Kelowna

Kelowna, British Columbia, Canada

London Health Sciences Centre - London Regional Cancer Program

London, Ontario, Canada

Odette Cancer Centre - Sunnybrook Health Sciences Centre

Toronto, Ontario, Canada