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Analysis of Hematoma Following Breast Surgery

U

University of Regensburg (UR)

Status

Completed

Conditions

Postoperative Bleeding
Hematoma

Treatments

Diagnostic Test: Closed-suction drain fluid volume

Study type

Observational

Funder types

Other

Identifiers

NCT03515525
18-955-104

Details and patient eligibility

About

A retrospective review of patients who developed hematoma following breast surgery from 2003 to 2018 in a single institution was performed. The study investigated the value of closed-suction drains regarding the quantity and quality of fluid secretion for the prediction of subcutaneous hematoma in patients undergoing breast surgery procedures.

Enrollment

20 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Patients who developed hematoma requiring revision following bilateral breast surgery including augmentation mammoplasty, subcutaneous mastectomy and breast reduction.

Exclusion criteria

  • Patients who developed hematoma requiring revision following unilateral breast surgery.
  • Breast surgery in absence of hematoma.
  • Patients with known coagulation disorders.

Trial design

20 participants in 2 patient groups

Hematoma side
Description:
Drain secretion volume prior to revision surgery on the breast side affected by hematoma.
Treatment:
Diagnostic Test: Closed-suction drain fluid volume
Non-hematoma side
Description:
Drain secretion volume prior to revision surgery on the breast side not affected by hematoma.
Treatment:
Diagnostic Test: Closed-suction drain fluid volume

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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