Actively Recruiting
Prospective Validation of the SWEET Tool for Pre-diction of Preintervention ERCP Procedure Time.
Led by Universitair Ziekenhuis Brussel · Updated on 2025-12-02
363
Participants Needed
1
Research Sites
104 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Endoscopic retrograde cholangiopancreatography (ERCP) is a frequently performed procedure worldwide. The procedure combines endoscopy and X-ray imaging to diagnose and treat problems in the bile and pancreatic ducts, most commonly stones or strictures. Until the recent publication of Waldthaler et al., there was little evidence about what patient- and procedure-related factors determine a priori the duration of an ERCP. Data from 74 248 ERCPs performed from 2010 to 2019 were extracted from the Swedish National Quality Registry (GallRiks) to identify variables predictive for ERCP time using linear regression analyses and root mean squared error (RMSE) as a loss function. Ten variables were combined to create an estimation tool for ERCP duration: the SWedish Estimation of ERCP Time (SWEET) tool. Having a predictive tool for estimating the procedure time of an invasive endoscopic procedure offers several valuable benefits across clinical, operational, and patient-centered domains: improved scheduling and resource allocation by optimized operating room and endos-copy suite scheduling, reduced delays and less overbooking or underutilization. It helps allocate the right number of staff (nurses, anesthesiologists) based on procedure complexity and minimizes unexpected extensions that lead to staff fatigue or overtime pay.
CONDITIONS
Official Title
Prospective Validation of the SWEET Tool for Pre-diction of Preintervention ERCP Procedure Time.
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age > 18 years
- First or redo-ERCP
- Intraductal endoscopy
- ERCPs performed by fellows under supervision
You will not qualify if you...
- ERCPs in altered anatomy
- ERCPs combined with therapeutic EUS interventions
AI-Screening
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Trial Site Locations
Total: 1 location
1
UZ Brussel
Brussels, Belgium
Actively Recruiting
Research Team
H
Helena Degroote, MD, PhD
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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