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Hemopatch Versus Axillary Drainage After Axillary Lymphadenectomy

Hemopatch Versus Axillary Drainage After Axillary Lymphadenectomy: Randomized, Controlled, Multicenter Clinical Study

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04487561
Acronym
REDHEMOPACH
Enrollment
228
Registered
2020-07-27
Start date
2020-03-01
Completion date
2023-02-14
Last updated
2023-02-17

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

Conditions

Breast Cancer, Breast-conserving Surgery, Axillary Lymph Node Dissection

Keywords

aspirative drainage, hemopatch, seroma, breast cancer

Brief summary

Aspirative drainage continues to be the gold standard for the management of this post-surgical complication, even though it can lead to complications such as obstruction of the drainage, peritubal leakage of the seroma, etc. This may result in pain and reduction in mobility of the affected arm. Based on our positive clinical outcomes and the fact that there is not any published data available in the literature regarding this use of the patch, the investigators propose a multicentric, randomized controlled clinical trial, with the objective of comparing the Hemopatch® with the usual technique used (aspirative drainage) in terms of efficacy and safety. Hypothesis: Placing a Hemopatch ® instead of an aspirative drainage in women after undergoing axillary lymph node dissection during breast cancer surgery may reduce the appearance of seroma and consequently the need for a puncture, as well as the complications related to aspirative drainage.

Detailed description

1. Introduction: In the surgical management of breast cancer, a conservative approach is the gold standard for the mammary region. For the axillary region, however, this depends on the results of the sentinel lymph node biopsy (SLNB) with axillary lymph node dissection (ALND) continuing to be an indispensable procedure when the disease reaches this level. The complications that arise from this procedure can be divided in two groups: 1) early: seromas and nerve lesions and 2) late: lymphedema, functional disorders in shoulder movement and post-mastectomy pain syndrome. Seromas are the most frequent complications after an ALND. In themselves, they do not carry a high risk of morbidity. However, they delay healing of the surgical wound, increasing the risk of infection and number of ambulatory visits and furthermore, resulting in a deferral in the start of adjuvant therapies such as radio and chemotherapy. Aspirative drainage continues to be the gold standard for the management of this post-surgical complication, even though it can lead to complications such as obstruction of the drainage, peritubal leakage of the seroma, etc. This may result in pain and reduction in mobility of the affected arm. Hemopatch® is a hemosthatic sealer made from reabsorbable collagen. It comes in the from of patch, with CE marking that is already being used in the clinical setting in Spain and the rest of Europe. Taking into account the factors that reduce seroma formation after ALND and the characteristics of the patch, its application after surgery could be useful in preventing seroma formation. More specifically, the patch has proven to act as a * Hemosthatic, improving the first phase of inflammation * Adhesive, reducing the dead space left after ALND * Sealer, decreasing the exudate 2. Rationale Based on this premise and in the context of a clinical protocol after the introduction of the patch in daily clinical practice, it was used on 28 patients that underwent ALND, obtaining favourable clinical results. This is a multicentric, randomized controlled clinical trial, with the objective of comparing the Hemopatch® with the usual technique used (aspirative drainage) in terms of efficacy and safety. 3. Hypothesis Placing a Hemopatch ® instead of an aspirative drainage in women after undergoing ALND during breast cancer surgery may reduce the appearance of seroma and consequently the need for a puncture, as well as the complications related to aspirative drainage.

Interventions

DEVICEhemopatch

The patient will be randomized after performing the lymphadenectomy, according to a table of random numbers performed in excel kuytools, then a compression bandage will be performed on all the patients and it will be controlled 24 hours postoperatively, the subsequent control will be weekly until the drain is removed. and / or the disappearance of the seroma

PROCEDUREAspirative drainage

The patient will be randomized after performing the lymphadenectomy, according to a table of random numbers performed in excel kuytools, then a compression bandage will be performed on all the patients and it will be controlled 24 hours postoperatively, the subsequent control will be weekly until the drain is removed. and / or the disappearance of the seroma

Sponsors

Fundación para la Investigación del Hospital Clínico de Valencia
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
SINGLE (Outcomes Assessor)

Intervention model description

Prospective multicentric randomized controlled clinical trial

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 99 Years
Healthy volunteers
No

Inclusion criteria

* Diagnosis of breast cancer, * scheduled for surgical treatment including conservative surgery and ALND. * Signed informed consent for ALND.

Exclusion criteria

* Selective sentinel node biopsy negative. * Subsidiary mastectomy patients. * Denial of informed consent for axillary lymphadenectomy.

Design outcomes

Primary

MeasureTime frameDescription
To develop seroma after surgeryPercentage, through study completion, an average of 2 monthsPercentage of patients that receive Hemopatch® that develop seroma after surgery and percentage of patients that receive that develop seroma after extraction of the aspirative drainage.
total volumen of the seromafrom 24 hours until there is no seroma, assessed up to 2 monthsThe initial control will be performed 24 hours after the intervention, maintaining AD if the volume is greater than 30ml. All patients will be seen 7 days after surgery. The follow-up time will be weekly until there is no seroma, measuring the volume of the seroma extracted by puncture,
Seroma puncturesthrough study completion, an average of 2 monthsthe total number of punctures needed
complicationsfrom 24 hours until there is no complications, assessed up to 2 monthsOther complications collected throughout the study include: bruising (yes / no), pain (yes / no), problems with aspiration drainage (yes / no)

Secondary

MeasureTime frameDescription
the coststhrough study completion, an average of 1 yearCompare the costs of both procedures by quantifying the costs of materials and consult time used in both procedures
body mass indexweight (kg) / height (m2). In the first consultationbody mass index
quality of life in patients1 week after surgery with Eortc QLQ-BR23Compare the quality of life in patients after receiving either of these procedures using the Eortc QLQ-BR23 survey

Countries

Spain

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 9, 2026