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Antibiotic Prophylaxis Before Percutaneous Gastrostomy

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University of Washington

Status

Completed

Conditions

Infection

Study type

Observational

Funder types

Other

Identifiers

NCT01424085
40912-B

Details and patient eligibility

About

The purpose of this study is to evaluate the use of antibiotics (i.e. Kefzol) before percutaneous gastrostomy performed in interventional radiology. Patient will be randomized to receive antibiotics or placebo before the procedure, and the rates of skin infection after the procedure will be determined between the two groups. This has never been studied in our population of patients undergoing the procedure. However, antibiotics are routinely given despite the lack of evidence. The investigators hypothesize that patient receiving prophylactic antibiotics will have a decreased number of infections compared to placebo.

Enrollment

124 patients

Sex

All

Ages

18 to 90 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Anyone over the age of 18 years who is not currently on antibiotics for other reasons

Exclusion criteria

  • Anyone on antibiotics for the treatment of other infections.
  • Anyone under the age of 18 years
  • Pregnant patients

Trial design

124 participants in 2 patient groups

Those receiving antibiotics
Description:
Patients who received one prophylactic dose of antibiotics.
Placebo
Description:
Patients who did not receive one prophylactic dose of antibiotics (received placebo).

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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