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Drains and Surgical Site Infections

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University Hospital Basel

Status

Completed

Conditions

Surgical Site Infection

Treatments

Procedure: Insertion of drainage

Study type

Observational

Funder types

Other

Identifiers

NCT03408782
ch10Weber

Details and patient eligibility

About

This prospective observational study examines the associations of presence, duration, type, number and location of surgical drains with the risk of surgical site infections in a contemporary and multicentric cohort of general, orthopedic trauma and vascular surgery procedures.

Full description

Surgical site infections (SSI) represent the most common type of nosocomial infection amongst surgical patients. They cause morbidity and mortality.

Surgical Drains are commonly inserted at the end of many surgical procedures. In contrast to potential benefits, drains are also thought to potentially serve as a conduit of bacteria into the wound and hence may increase the risk of SSI. Patterns of use of drains vary widely across surgical disciplines and individual practices. There are no uniform guidelines and standards are often rather based on tradition than on evidence. The aim of this large prospective study was to examine the association of presence, duration, type, number and location of drains with the risk of SSI in a contemporary and multicentric cohort of general, orthopedic trauma and vascular surgery procedures.

Enrollment

4,584 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Inpatients
  • Age 18 years or older
  • General, orthopedic trauma and vascular procedures
  • Surgical antimicrobial prophylaxis

Exclusion criteria

  • outpatient surgery
  • Presence of a contraindication for cefuroxime and/or metronidazole
  • preexisting antibiotic therapy within 14 days prior to surgery
  • cognitive impairment
  • combined operations including other than the above specified surgical divisions
  • Emergency procedures with planned incision within 2 hours after indicating the procedure.

Trial design

4,584 participants in 2 patient groups

No drainage
Description:
Those patients that underwent surgery and no drain was inserted at the end of the procedure
Drainage
Description:
Those patients that underwent surgery and one or several drains were inserted at the end of the procedure.
Treatment:
Procedure: Insertion of drainage

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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