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Post-Endoscopic Infection Rate Notifications to Improve the Delivery of Care

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Johns Hopkins University

Status

Completed

Conditions

Infection

Treatments

Other: Option 1: National comparison
Other: Option 2: National comparison with benchmarking

Study type

Interventional

Funder types

Other

Identifiers

NCT03922971
IRB00203304

Details and patient eligibility

About

This project will notify centers of center's post-endoscopic infection rates and evaluate the effectiveness of this notification system to decrease infection rates. The investigators aim to notify centers of the number of patients and center's risk-adjusted rates of hospitalizations for infections after colonoscopy and esophagogastroduodenoscopy (EGD) procedures performed between January 2015 and September 2018. The investigators will randomize centers to two notification groups: (1) Ability to view center's rate compared with all other centers (ASCs and outpatient centers notified and compared separately) or (2) Ability to view center's rate compared with the other centers with a similar patient comorbidity profile and in addition to viewing option 1. Facilities will answer questions about center's infection control practices. The investigators hypothesize that centers with high rates of post-procedural infections will (1) be more likely to report that the center took action to investigate the center's infection control practices after the first notification and (2) observe a decrease in infections after the notification. The investigators anticipate that centers with high rates of post-procedural infections that are randomized to group 2 will have greater change. The investigators anticipate no change in rates of infection in the facilities that had zero or very low (n=1) event rates.

Enrollment

303 patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Facilities that bill to fee for service Medicare for gastrointestinal endoscopy

Exclusion criteria

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

303 participants in 2 patient groups

National comparison
Other group
Description:
Ability to view center's rate compared with all others
Treatment:
Other: Option 1: National comparison
National comparison with benchmarking
Other group
Description:
Ability to view center's rate compared with the others with a similar patient comorbidity profile and in addition to viewing option 1
Treatment:
Other: Option 2: National comparison with benchmarking

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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