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Shorter radiation for breast cancer: 2 weeks vs 3 weeks – which is better?

NCT ID NCT07344597

Disease control Sponsor: Salwa Shawky Bakeet Ali Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting This study
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study compares two shortened radiation therapy schedules for breast cancer patients after surgery: one lasting 2 weeks and another lasting 3 weeks. The goal is to see which schedule better controls the cancer and causes fewer skin side effects. About 70 women who have had breast-conserving surgery or mastectomy will participate.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Participants

About 70 people

The number the study aims to enrol. It can still change while the study runs.

Expected to start

Jan 2026

An estimate. Start dates often move.

Expected to finish

Feb 2027

An estimate. End dates often move.

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Who is studied

breast cancer patients above 18y,with invasive carcinoma,excision of primary,recieved neoadjuvant or adj cth .

Ages

18 to 100 years

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Female patients aged ≥18 years. Female or male patients with invasive carcinoma of the breast. Complete microscopic excision of primary tumor. Undergoing breast-conserving surgery (BCS) or modified radical mastectomy (MRM). ≥ Axillary lymph nodes dissected. T1\_4pN0\_3M0 disease. Neoadjuvant or adjuvant CTH . Signed informed consent and able to comply with follow up. Exclusion Criteria: * Evidence of distant metastases. Past history of malignancy. Prior radiotherapy to the chest region Simultaneous malignancy (except non-melanoma skin cancer or in situ cervical carcinoma) Connective tissue diseases (e.g., lupus erythematosus, scleroderma) Pregnancy or lactation

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Conditions

The condition(s) this trial relates to.

breast cancer breast neoplasm

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Breast cancer

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. A doctor treating you

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

Contacts and locations

Locations

  • Assuit

    Asyut, Egypt

More trials for these conditions

Other studies related to the condition(s) this trial covers.