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The INSPIRE-ASP UTI Trial

Harvard Pilgrim Health Care logo

Harvard Pilgrim Health Care

Status

Completed

Conditions

Urinary Tract Infection (UTI)

Treatments

Other: INSPIRE CPOE Smart Prompt
Other: Routine Care

Study type

Interventional

Funder types

Other
Other U.S. Federal agency
Industry

Identifiers

NCT03697096
PH000619B_UTI

Details and patient eligibility

About

The INSPIRE-ASP UTI trial is a cluster-randomized controlled trial of HCA hospitals comparing routine empiric antibiotic stewardship practices with real-time precision medicine computerized physician order entry smart prompts providing the probability that a non-critically ill adult admitted with UTI is infected with a resistant pathogen.

Note: that enrolled "subjects" represents 59 individual HCA hospitals that have been randomized.

Enrollment

55,412 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Facility Inclusion Criteria:

  • HCA hospitals admitting adults for UTI
  • Facility use of MEDITECH as their electronic health record system

Facility Exclusion Criteria:

Note: unit of randomization is the hospital, however the CPOE alert intervention will calculate risk estimates for adults age >=18 admitted to non-ICU wards and who are ordered to receive extended-spectrum antibiotics for UTI. Prisoners were excluded from prompts and analysis.

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

55,412 participants in 2 patient groups

Routine Care
Active Comparator group
Description:
Continued routine antibiotic stewardship strategies.
Treatment:
Other: Routine Care
INSPIRE CPOE Smart Prompt
Active Comparator group
Description:
Use of a computerized physician order entry (CPOE) smart prompt alert to guide empiric choice of antibiotics for UTI in non-ICU patients in the first 3 days of hospitalization.
Treatment:
Other: INSPIRE CPOE Smart Prompt

Trial documents
2

Trial contacts and locations

59

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Data sourced from clinicaltrials.gov

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