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NCT03922971 · ClinicalTrials.gov registry record · NA
Post-Endoscopic Infection Rate Notifications to Improve the Delivery of Care
A NA study, sponsored by Johns Hopkins University.
- Completed
- Registry status
- NA
- Development phase
- 303
- Enrollment target
NCT03922971: Completed NA study, sponsored by Johns Hopkins University.
NCT03922971 is a NA study that has completed, run by Johns Hopkins University. The registered enrollment target is 303 participants. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT03922971, a NA study, has completed, sponsored by Johns Hopkins University.
- COMPLETED
- Registry status
- NA
- Development phase
- 303 participants
- Enrollment target
Study Summary
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.
Interventions
- OTHER Option 1: National comparison
- OTHER Option 2: National comparison with benchmarking
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 303 participants |
| Start Date | 2019-08-07 |
| Est. Completion | 2023-06-15 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT03922971
The ClinicalTrials.gov registry entry for NCT03922971 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 303 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Johns Hopkins University, which has 1,448 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Option 1: National comparison is the first listed.
NCT03922971 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT03922971 about?
NCT03922971 is a clinical study titled "Post-Endoscopic Infection Rate Notifications to Improve the Delivery of Care". 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 a...
What is the current status of trial NCT03922971?
This trial is currently completed. It is a NA study. The enrollment target is 303 participants. The study started on 2019-08-07. Estimated completion is 2023-06-15.
What interventions are being tested in trial NCT03922971?
The interventions under investigation include: Option 1: National comparison (OTHER), Option 2: National comparison with benchmarking (OTHER).
Who is sponsoring clinical trial NCT03922971?
This trial is sponsored by Johns Hopkins University, which has 1,448 total clinical trials registered on ClinicalTrials.gov.
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