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OncoMatch/Clinical Trials/NCT07711847

Personalized Prone Immobilization for Accelerated Partial Breast Radiotherapy

Is NCT07711847 recruiting? Yes, currently enrolling (Sep 2026). This NA trial studies VENUS SHELL™ immobilization device for invasive breast cancer early stages.

NARecruitingHeroSupport SANCT07711847Data as of Sep 2026

Treatment: VENUS SHELL™ immobilization deviceThe goal of this clinical trial is to find out whether using a personalized breast holder (called VENUS SHELL™) can improve positioning and patient comfort during prone radiotherapy (radiotherapy given while the patient lies on her stomach). The main goals of the study are: * To confirm that using the VENUS SHELL™ is safe and effective * To assess whether the VENUS SHELL™ helps deliver accurate radiation treatment in a faster and more comfortable way Participants will: * Attend a study visit before radiotherapy to have a breast surface scan (no radiation) and enable the production of their personalized VENUS SHELL™ * Use their VENUS SHELL™ during radiotherapy planning and treatment * Be asked to complete questionnaires about their comfort

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Extracted eligibility criteria

Treatments studied

Other

VENUS SHELL™ immobilization device

Cancer type

Breast Carcinoma

Biomarker criteria

Excluded: BRCA1 mutation

Known germline BRCA1/2 mutation

Excluded: BRCA2 mutation

Known germline BRCA1/2 mutation

Disease stage

Required: Stage PT1, PT2, PTIS (other)

Staging pT1-T2, N0M0 (Tumor size ≤3 cm); Staging pTis (tumor size ≤3 cm)

Performance status

ECOG 0–2(Ambulatory, capable of self-care)

ECOG/WHO performance status ≤2

Demographics

Ages ≥ 40
Female only

Prior therapy

Must have received: breast conservative surgery

Upfront breast conservative surgery

Structured fields extracted by AI. May contain errors — verify against the official protocol.

US trial sites

  • NYU Grossman School of Medicine · New York, New York

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Frequently asked questions

Is NCT07711847 currently recruiting?

Yes, this trial is currently recruiting patients.

Is prior treatment required for enrollment?

Yes. Patients must have previously received breast conservative surgery.

Are patients with BRCA1 alterations eligible?

No. BRCA1 mutation is an exclusion criterion.

Are patients with BRCA2 alterations eligible?

No. BRCA2 mutation is an exclusion criterion.

What disease stage is eligible?

Stage PT1 or PT2 or PTIS is required.

Is this trial open to male patients?

No. This trial enrolls female patients only.

Could you qualify for this trial?

Enter your biomarker results to see how this trial's eligibility criteria match your specific cancer profile.

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