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Comparison Of Hypofractionated And Conventional Radiotherapy In Advanced Breast Cancer

Comparison Of Local Control And Complications Of Hypofractionated Radiotherapy With Conventional In Patients With Advanced Breast Cancer

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20250728066668N1
Enrollment
200
Registered
2025-08-01
Start date
2025-08-06
Completion date
Unknown
Last updated
2025-08-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Breast Cancer. Malignant neoplasm of breast

Interventions

Intervention 1: Intervention Group:Patients with advanced breast cancer undergo hypofractionated radiotherapy treatment for three weeks. During treatment, they are monitored weekly for complications b

Sponsors

Babol University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: All Patients With Advanced Breast Cancer And Confirmed Histologic Diagnosis With Negative Surgical Margin

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Acute Complication of Hypofraction And Conventional. Timepoint: Patients will be seen weekly during radiotherapy and once a month afterwards for treatment complications. Method of measurement: A checklist designed based on CTCAE v5.0 (radiotherapy-induced dermatitis), RTOG (subcutaneous toxicity) and SOMA/LENT (telangiectasia, hand edema, pain in the radiotherapy area) will be completed to review the complications of interest.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactNajme Radmard

Babol University of Medical Sciences

Radmardnajme1@gmail.com+98 11 3219 9592

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026