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Breast NeoplasmsAMBULANTNCT02187718

Ambulatory SNP Under Local Anaesthesia in a Subgroup of Breast Cancer Patients - Trial

A study testing Sentinel Node Procedure under Local Anaesthesia and Sentinel Node Procedure under General Anaesthesia in people with Breast Neoplasms, run by Medical Center Alkmaar at 1 site in Netherlands.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

Rationale: In breast cancer (BC) patients, lymph node status is a key prognostic indicator. At present, axillary ultrasound (US) with subsequent fine needle aspiration cytology (FNAC) of suspicious lymph nodes (US+FNAC) is widely used as a pre-operative staging method. Read more about this study

Who is it for?
Ages 18 to 60 years, women only
Conditions the study is for
Breast Neoplasms
What is being tested?
Sentinel Node Procedure under Local Anaesthesia and Sentinel Node Procedure under General Anaesthesia
Type of treatment
Surgery or procedure
Could I receive a placebo?
No, everyone receives an active treatment
How many people
80 participants
Where
1 siteNetherlands
Study dates
Jan 2015to Aug 2017
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 60 years
  • Women only
  • No healthy volunteers
  • Adult

Who may be able to join

  • Female
  • Age 18-60 years
  • Diagnosis of invasive BC (established with core needle biopsy of the breast lesion)
  • Breast carcinoma measures > 20 mm ultrasonographically
  • Pre-operative US+FNAC is negative or inconclusive
  • No evidence of distant metastases
  • ASA Classification I-III
  • Signed informed consent

Who cannot join

  • History of previous breast surgery in the affected breast
  • History of previous axillary surgery in the ipsilateral axilla
  • History of radiation therapy (ipsilateral breast or axilla)
  • History of neo-adjuvant therapy (for the BC)
  • Known allergy to lidocain

Trial locations and contacts

1 site in 1 country.

Martijn Leenders, MD contact

+31624271275

m.w.h.leenders@mca.nl

Hermien Schreurs, MD, PhD contact

+31725484444

w.h.schreurs@mca.nl

Netherlands1 site
  • Medical Center Alkmaar

    Alkmaar, North Holland

    Martijn Leenders, MD

    Hermien Schreurs, MD, PhD

Other trials in Netherlands

About this study

Official title: A Prospective Single-centre Randomised Controlled Clinical Trial Comparing Sentinel Node Procedure Under Local Anaesthesia to Traditional Sentinel Node Procedure Under General Anaesthesia in Patients <60 Years With a Breast Carcinoma >20 mm.

Rationale: In breast cancer (BC) patients, lymph node status is a key prognostic indicator. At present, axillary ultrasound (US) with subsequent fine needle aspiration cytology (FNAC) of suspicious lymph nodes (US+FNAC) is widely used as a pre-operative staging method. When US+FNAC is negative, a sentinel node procedure (SNP) is performed during breast surgery. Nowadays, an axillary lymph node dissection (ALND) is generally performed if one of the abovementioned diagnostic entities reveals lymph node metastases. However, the extensive role of ALND in BC patients with lymph node metastases may change or diminish in upcoming years due to emerging evidence that completion ALND (cALND) does not affect disease-free survival and overall survival in early BC patients with (sentinel) node-positive disease. Whether ALND is needed in these patients, should be based on (axillary) tumour load. Because of the fact that tumour load can only be reliably evaluated by SNP and not by US+FNAC, the role of SNP might become even more important in upcoming years.

Ideally, the status of this sentinel lymph node is known prior to breast surgery, so a patient tailored treatment plan can be made and discussed with the patient before breast surgery. In this context, it would be very logical to perform a SNP under local anaesthesia (LA), prior to breast surgery. This might not only lead to significantly less two-step surgical procedures under general anaesthesia (GA), but might also lead to a reduction of depressive symptoms and anxiety and improved quality of life (QoL) of BC patients, because BC patients are in particular risk for psychological distress in the first three months after diagnosis of BC. Knowing lymph node status and the complete treatment plan as soon as possible (by performing a SNP under LA), might reduce this psychological distress. To investigate which BC patients would benefit most from SNP under LA, the investigators recently analysed 1132 BC patients retrospectively. Both prevalence of axillary lymph node metastases and prevalence of false negative results of US+FNAC were directly associated with age <60 years and with primary breast tumour size >20 mm. Hence, these BC patients might benefit most from SNP under LA. In the present study, the value of SNP under LA in these BC patients (i.e. <60 years with a breast carcinoma >20 mm) will be analysed.

Read more

Objectives: Reduction of the mean number of operations under general anaesthesia per patient. Improvement of QoL. Reduction of depressive symptoms and experienced anxiety.

Study design: Prospective single centre randomised controlled clinical trial. Study population: Women aged 18 to 60 years who are diagnosed with BC AND with a tumour size of >20 mm ultrasonographically AND with a negative or inconclusive pre-operative US+FNAC.

Intervention: Sentinel Node Procedure under Local Anaesthesia (SNP under LA) Control: Traditional Sentinel Node Procedure under General Anaesthesia (SNP under GA) Main study parameters: Primary outcome parameters are the number of operations under GA per patient and the number of operations under LA per patient. Secondary outcome parameters are QoL, experienced depressive symptoms and anxiety.

Timeline and statistics: The inclusion period will be conducted from the 1st of July 2014 to the 1st of August 2015, and 80 patients will be enrolled in this study (alpha 0.05; power 0.8). Inclusion of 80 patients will be sufficient to reduce the number of two-stage surgical procedures under general anaesthesia with 30%. Data will be analysed using descriptive statistics, Chi-squared test, Fisher's exact test, Mann-Whitney U test, Kruskall-Wallis test, students t-test, ANOVA, paired t-test, Wilcoxon signed-rank test, Friedman test, Pearson's and Spearman's rank correlation coefficients and finally logistic and linear regression analysis.

Being tested
Sentinel Node Procedure under Local Anaesthesia, Sentinel Node Procedure under General Anaesthesia
Keywords
Sentinel Lymph Node Biopsy, Local Anaesthesia
Medical subject headings
Breast Neoplasms

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Sentinel Node Procedure under Local AnaesthesiaProcedure or surgery

  • Sentinel Node Procedure under General AnaesthesiaProcedure or surgery

Study groups in NCT02187718
Study groupRoleWhat they receive
SNPGAOtherSentinel Node Procedure under General Anaesthesia
Receives: Procedure: Sentinel Node Procedure under General Anaesthesia
SNPLAOtherSentinel Node Procedure under Local Anaesthesia
Receives: Procedure: Sentinel Node Procedure under Local Anaesthesia

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Number of operations under general anaesthesia

    Measured: 6 months

  2. Number of operations under local anaesthesia

    Measured: 6 months

  3. The number of patients in whom breast surgery is performed ≤21 days.

    Measured: 6 months

Secondary outcomes (3)
  1. Quality of Life

    Quality of Life is measured with the WHOQOL-bref questionnaire

    Measured: 6 months

  2. Depressive symptoms

    Depressive symptoms are measured with the Centre for Epidemiological Studies-Depression scale (CES-D)

    Measured: 6 months

  3. Anxiety

    Anxiety is measured with the State-and-Trait-Anxiety-Inventory (STAI)

    Measured: 6 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted11 Jul 2014 (estimated)
  2. Study startJan 2015
  3. Primary completionDec 2016 (estimated)
  4. Study completionAug 2017 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Diagnosis
Allocation
Randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
80 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT02187718
Sponsor's protocol ID
NL49489.094.14
Acronym
AMBULANT
Status last verified
Jul 2014
First submitted
9 Jul 2014
Last updated
11 Jul 2014
Results posted
No
Data monitoring committee
No

Questions about this trial

What is this clinical trial studying?

A study testing Sentinel Node Procedure under Local Anaesthesia and Sentinel Node Procedure under General Anaesthesia in people with Breast Neoplasms, run by Medical Center Alkmaar at 1 site in Netherlands.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 8 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 11 Jul 2014. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Netherlands. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

Contact Martijn Leenders, MD (+31624271275, m.w.h.leenders@mca.nl), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Number of operations under general anaesthesia (time frame: 6 months). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 11 Jul 2014.

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