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Sentinel Node And Recurrent Breast cancer

Sentinel Node And Recurrent Breast cancer

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON22722
Enrollment
150
Registered
2008-09-18
Start date
2008-03-01
Completion date
Unknown
Last updated
2024-02-28

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

Conditions

Recurrent breast cancer Sentinel node biopsie Recidief mammacarcinoom Schildwachtklierprocedure

Interventions

Lymfatic Mapping and sentinel lymph node biopsie.

Sponsors

The principal investigator of this study is mrs. A. Maaskant-Braat, resident surgery
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Women above 18 years old with locally recurrent breast cancer after earlier BCT or modified radical mastectomy. 2. Operable cytological /histological confirmed locally recurrent breast cancer. 3. Having obtained an informed consent.

Exclusion criteria

Exclusion criteria: 1. Proven ipsi- or contralateral regional lymph node metastases (ultrasound and FNA). 2. Known to be allergic to “99mTc-colloidal albumin” or blue dye injection fluids.

Design outcomes

Primary

MeasureTime frame
- Registration of technical feasibility of lymphatic mapping and sentinel node biopsy in patients with locally recurrent breast cancer. - Registration of success rate of lymphatic mapping and SNB in patients with locally recurrent breast cancer. - Registration of validity of lymphatic mapping and sentinel node biopsy in patients with locally recurrent breast cancer.

Secondary

MeasureTime frame
- Registration of lymphatic drainage pathways in patients with locally recurrent breast cancer. - Registration of sentinel lymph node status in patients with locally recurrent breast cancer. - Registration of possible influence of lymphatic mapping and SNB on therapeutic decisions in patients with locally recurrent breast cancer.

Contacts

Public ContactA. Maaskant-Braat

Catharina ziekenhuis Eindhoven Afdeling chirurgie

SNARBgroup@gmail.com+31 (0)40 2399111 / 7174

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)