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Clinical Trials/NCT03305757
NCT03305757CompletedPhase 4

A Multi-center, Double Blinded Randomized Controlled Trial Evaluating Closure of the Dead Space After Mastectomy Using Sutures or Tissue Glue Versus Conventional Closure. Protocol for the Seroma Reduction After Mastectomy (SAM) Trial

Zuyderland Medisch Centrum1 site in 1 country339 target enrollmentStarted: June 1, 2014Last updated:
Conditions
Interventions
Drugs

Trial Snapshot

Phase
Phase 4
Status
Completed
Sponsor
Enrollment
339
Locations
1
Primary Endpoint
Number of seroma aspirations

Study Overview

Brief Summary

Rationale: Seroma formation and its sequelae form the mainstay of complications in breast cancer surgery. Seroma has an incidence of 3% to 85%. Complications vary from delayed wound healing, infection, skin flap necrosis, patient discomfort and repeated visits to the out patient clinic. The key to reducing seroma formations seems to partly lie in the obliteration of dead space. The use of electrocautery has been demonstrated to increase seroma formation following mastectomy, however no other surgical devices (laser scalpel, argon diathermy and ultrasonic scalpel) or substances have proven to be superior in seroma reduction.

No prospective randomized controlled trials have been able to demonstrate which techniques are superior in reducing seroma and as a consequence patient discomfort in patients undergoing mastectomy. In a previous retrospective observational study these investigators demonstrated that mastectomy flap fixation significantly reduced seroma formation and the number of seroma aspirations. In a pilot study that was recently performed in one of the investigators hospitals, ARTISS tissue glue was used for skin flap fixation and showed promising results. The investigators hypothesize that obliteration of the dead space following mastectomy will significantly reduce seroma formation, its complications and the discomfort it causes patients undergoing mastectomy.

Detailed Description

  1. INTRODUCTION AND RATIONALE

Seroma formation is a common side effect after surgery for breast cancer, with an incidence of 3% to 85%. Seroma is a collection of serous fluid that contains blood plasma and/ or lymph fluid. Some surgeons regard seroma formation as a necessary evil after breast cancer surgery. Seroma formation and its sequelae form the mainstay of complications in breast cancer surgery. Complications vary from delayed wound healing, infection, skin flap necrosis, patient discomfort and repeated visits to the out patient clinic to deal with seroma and its sequelae.

The key to reducing seroma formations seems to partly lie in the obliteration of dead space. However, the techniques used to achieve this goal are subjects of much controversy and debate. In a randomized controlled study it was difficult to elucidate whether reducing the dead space or ligation of lymphatics or a combination of both were responsible of reduction of seroma formation.

The use of electrocautery has been demonstrated to increase seroma formation following mastectomy, however no other surgical devices (laser scalpel, argon diathermy and ultrasonic scalpel) or substances have proven to be superior in seroma reduction. Seroma formation after axillary dissection for breast cancer cannot be avoided but hopefully it can be minimized by mechanical dead space closure. This systematic review highlights the fact that seroma formation is multifactorial and prevention of seroma is difficult at present. Certain prospective trials have been performed that demonstrate that flap anchoring and therefore dead space reduction could be very beneficial. The trial performed by Laurence et al analysed flap fixation and closed suction drainage. In this study there was no difference in seroma rates, but patients without drains were discharged earlier. In the trial performed by Sakkary et al the amount of fluid drained was significantly less in the flap fixation group however patient discomfort (seroma aspirations and out patient visits) were not assessed.

A Cochrane review was published in 2013 regarding Fibrin Glue (Tissuecol), Fibrin Glue did not influence the incidence of postoperative seroma, the mean volume of seroma, wound infections, complications and the length of hospital stays in people undergoing breast cancer surgery. Due to significant methodological and clinical diversity among the included studies this conclusion may be considered weak and biased. Therefore, a major multicentre and high-quality RCT is required to validate these findings. ARTISS tissue glue is a two-component fibrin sealant matrix of human fibrinogen and human thrombin wich has the advantage of setting in 60 seconds. This means that the surgeon has 60 seconds to correctly position the skin flaps before the tissue sealant sets,

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Triple (Participant, Care Provider, Investigator)

Masking Description

Randomisation is achieved using a web based randomization programme (RANDI2). Randomization will take place on the day of surgery, after the start of the operation and 30 minutes before wound closure. Blocked randomisation will take place with randomly selected block sizes (6/9/12) with an allocation ratio of 1:1:1. Randomisation will be stratified per site. Both patients and surgeons will be blinded. Patients will be informed preoperatively that their post-operative check ups will NOT be performed by the surgeon that performed the surgery. Randomisation will take place 30 minutes before wound closure in the operating theatre. Post-operatively, patients will not be evaluated by their own surgeon. The OR report will contain the following information (in Dutch) so as to ensure that blinding of the physicians will not be compromised.

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
Female
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Older than 18 years
  • Female sex
  • Indication for mastectomy or modified radical mastectomy

Exclusion Criteria

  • Patients undergoing breast conserving therapy
  • Patients undergoing direct breast reconstruction
  • Unable to comprehend implications and extent of study and sign for informed consent

Arms & Interventions

conventional wound closure

Active Comparator

The skin flaps will not undergo further treatment in this group.

Intervention: Conventional (Procedure)

flap fixation with vicryl sutures

Experimental

The skin flaps will be sutured on to the pectoral muscle after having performed the mastectomy.

Intervention: vicryl sutures (Procedure)

Artiss tissue glue

Experimental

ARTISS tissue glue will be applied to the skin flaps after mastectomy

Intervention: Artiss (Drug)

Outcomes

Primary Outcomes

Number of seroma aspirations

Time Frame: 1 year following surgery

Number of seroma aspirations performed post mastectomy

Secondary Outcomes

  • Infection rate(1 year following surgery)
  • Cosmesis(1 year following surgery)
  • Impact on Quality of life(1 year following surgery)
  • Shoulder function(1 year following surgery)
  • Number of out patient clinic visits(1 year following surgery)
  • Cost effectiveness(1 year following surgery)

Investigators

Sponsor
Zuyderland Medisch Centrum
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

James van Bastelaar

MD

Zuyderland Medisch Centrum

Study Sites (1)

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