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Do Closed Suction Drains Affect the Complications Rate of Breast Reconstruction With Silicone Prosthesis?

S

Sheba Medical Center

Status

Unknown

Conditions

Breast Reconstruction

Treatments

Other: Cultures taken from the drain discharge

Study type

Observational

Funder types

Other

Identifiers

NCT00973544
SHEBA -08-5530 -EW- CTIL

Details and patient eligibility

About

The purpose of this study is to describe the relations between closed suction drains placement in breast reconstructions procedures with silicone prothesis to the development of local wound complications (seroma, hematoma, infections).

Full description

Breast reconstruction with silicone prosthesis can be divided into two groups: immediate and late reconstructions. The complications rates reported in the literature are around 30% for delayed reconstructions and 50% for immediate reconstructions. The estimated surgical site infection rate is approximately 7% and seroma formation rate is approximately 1.2%.

In many of the procedures closed suction drains are left for fluid drainage, in order to reduce seroma formation. Still, the timing of drains' removal is controversial. Our aim in this study is to describe the relation between the placement of closed suction drains, the timing for their removal, and immediate post operative complications.

Patients that underwent breast reconstruction with silicone prosthesis and in which drains will be left in the surgical field would be randomly assigned into two groups: a control group, in which drains will be removed when the daily discharge will be below 20 cc for two consecutive days and the study group, in which drains will be removed on post operative day (POD) 10. All patients will receive the same antibiotic prophylaxis regimen. Cultures will be taken from fluid discharge POD 4,8,10 and 12. The incidence of local wound complications such as infection, seroma, hematoma and skin necrosis was record and analyzed.

Enrollment

100 estimated patients

Sex

Female

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • patients that underwent immediate or late breast reconstruction with silicone prosthesis (expanders/implants)and in which closed suction drains were left in the operating field according to the decision of the operating surgeon.
  • signature of informed consent form

Exclusion criteria

  • age under 18
  • breast reconstruction without prosthesis
  • Breast reconstruction without the use of drains
  • Active infection during time of surgery in surgical site
  • Coagulation disease
  • Psychiatric illness
  • Immune disease
  • Lack of communication or language problems
  • Foreign residents, not Israeli citizens
  • Prisoners

Trial design

100 participants in 2 patient groups

control
Description:
drains would be removed when daily discharge will be below 20 cc for 2 consecutive days
Treatment:
Other: Cultures taken from the drain discharge
study
Description:
drains will be removed on post operative day (POD) 10
Treatment:
Other: Cultures taken from the drain discharge

Trial contacts and locations

0

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Central trial contact

Eyal Winkler, MD; Hadar Israeli, MD

Data sourced from clinicaltrials.gov

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