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Prospective Validation of the SWEET Tool for Pre-diction of Preintervention ERCP Procedure Time.

U

Universitair Ziekenhuis Brussel

Status

Enrolling

Conditions

Endoscopic Retrograde Cholangio-Pancreatography

Treatments

Procedure: ERCP

Study type

Observational

Funder types

Other

Identifiers

NCT07259395
TIME SWEET

Details and patient eligibility

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.

Enrollment

363 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age > 18 years
  • First or redo-ERCP
  • Intraductal endoscopy
  • ERCPs performed by fellows under supervision

Exclusion criteria

  • ERCPs in altered anatomy
  • ERCPs combined with therapeutic EUS interventions

Trial design

363 participants in 1 patient group

ERCP group
Treatment:
Procedure: ERCP

Trial contacts and locations

1

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Central trial contact

Helena Degroote, MD, PhD

Data sourced from clinicaltrials.gov

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