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Hemopatch Versus Axillary Drainage After Axillary Lymphadenectomy (REDHEMOPACH)

Primary Purpose

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

Status
Completed
Phase
Not Applicable
Locations
Spain
Study Type
Interventional
Intervention
hemopatch
Aspirative drainage
Sponsored by
Fundación para la Investigación del Hospital Clínico de Valencia
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Breast Cancer focused on measuring aspirative drainage, hemopatch, seroma, breast cancer

Eligibility Criteria

18 Years - 99 Years (Adult, Older Adult)FemaleDoes not accept healthy volunteers

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.

Sites / Locations

  • Hospital Clínico Universitario de Valencia

Arms of the Study

Arm 1

Arm 2

Arm Type

Other

Active Comparator

Arm Label

aspirative drainage

Hemopatch

Arm Description

Drainage is the usual treatment after axillary lymphadenectoma for breast cancer

The hemopatch group will be the group without drainage and with a product patch

Outcomes

Primary Outcome Measures

To develop seroma after surgery
Percentage 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 seroma
The 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 punctures
the total number of punctures needed
complications
Other complications collected throughout the study include: bruising (yes / no), pain (yes / no), problems with aspiration drainage (yes / no)

Secondary Outcome Measures

quality of life in patients
Compare the quality of life in patients after receiving either of these procedures using the Eortc QLQ-BR23 survey
the costs
Compare the costs of both procedures by quantifying the costs of materials and consult time used in both procedures
body mass index
body mass index

Full Information

First Posted
July 7, 2020
Last Updated
February 16, 2023
Sponsor
Fundación para la Investigación del Hospital Clínico de Valencia
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1. Study Identification

Unique Protocol Identification Number
NCT04487561
Brief Title
Hemopatch Versus Axillary Drainage After Axillary Lymphadenectomy
Acronym
REDHEMOPACH
Official Title
Hemopatch Versus Axillary Drainage After Axillary Lymphadenectomy: Randomized, Controlled, Multicenter Clinical Study
Study Type
Interventional

2. Study Status

Record Verification Date
February 2023
Overall Recruitment Status
Completed
Study Start Date
March 1, 2020 (Actual)
Primary Completion Date
February 14, 2023 (Actual)
Study Completion Date
February 14, 2023 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Fundación para la Investigación del Hospital Clínico de Valencia

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

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
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 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. 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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Breast Cancer, Breast-conserving Surgery, Axillary Lymph Node Dissection
Keywords
aspirative drainage, hemopatch, seroma, breast cancer

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Prospective multicentric randomized controlled clinical trial
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
228 (Actual)

8. Arms, Groups, and Interventions

Arm Title
aspirative drainage
Arm Type
Other
Arm Description
Drainage is the usual treatment after axillary lymphadenectoma for breast cancer
Arm Title
Hemopatch
Arm Type
Active Comparator
Arm Description
The hemopatch group will be the group without drainage and with a product patch
Intervention Type
Device
Intervention Name(s)
hemopatch
Intervention Description
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
Intervention Type
Procedure
Intervention Name(s)
Aspirative drainage
Intervention Description
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
Primary Outcome Measure Information:
Title
To develop seroma after surgery
Description
Percentage 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.
Time Frame
Percentage, through study completion, an average of 2 months
Title
total volumen of the seroma
Description
The 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,
Time Frame
from 24 hours until there is no seroma, assessed up to 2 months
Title
Seroma punctures
Description
the total number of punctures needed
Time Frame
through study completion, an average of 2 months
Title
complications
Description
Other complications collected throughout the study include: bruising (yes / no), pain (yes / no), problems with aspiration drainage (yes / no)
Time Frame
from 24 hours until there is no complications, assessed up to 2 months
Secondary Outcome Measure Information:
Title
quality of life in patients
Description
Compare the quality of life in patients after receiving either of these procedures using the Eortc QLQ-BR23 survey
Time Frame
1 week after surgery with Eortc QLQ-BR23
Title
the costs
Description
Compare the costs of both procedures by quantifying the costs of materials and consult time used in both procedures
Time Frame
through study completion, an average of 1 year
Title
body mass index
Description
body mass index
Time Frame
weight (kg) / height (m2). In the first consultation

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
99 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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.
Facility Information:
Facility Name
Hospital Clínico Universitario de Valencia
City
Valencia
ZIP/Postal Code
46010
Country
Spain

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
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29658322
Citation
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Links:
URL
http://www.eortc.org
Description
Survey of Eortc QLQ- BR23
URL
http://www.ncbi.nlm.nih.gov/pubmed/16286909
Description
Pathophysiology of seroma in breast cancer. Breast Cancer [Internet]. 2005;12(4):288-93.

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Hemopatch Versus Axillary Drainage After Axillary Lymphadenectomy

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