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Not yet recruitingNCT05798065ImpatienceUpdated Nov 21, 2024

Inpatient Endoscopy Procedure Planning Delays and Impact on Length of Stay and 30-day Readmission

An observational study in Inpatient Endoscopy Delay, Readmission and Prolonged Hospital Stay, sponsored by Radboud University Medical Center. Not yet recruiting at 1 site in Netherlands. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2024-11-21.

Sponsored by Radboud University Medical Center · Observational

From the registry’s dates

  • Primary completion was expected by Jun 2025, 1 year 3 months ago, but the record still lists the study as not yet recruiting.
Study type
Observational
Model
Cohort
Time perspective
Retrospective
Enrollment
3,700
Ages
18 Years and older
Sex
All
01

Study summary

Single center retrospective cohort study of all inpatient endoscopy procedures to asses factors associated with inpatient endoscopy delays and impact on length of stay and 30-day readmission

Read the detailed description

Background: Delays in inpatient endoscopy planning negatively influence the quality and accessibility of care. This may result in higher healthcare costs, negative health outcomes, and unnecessary readmissions and use of hospital beds. Additionally, prolonged hospital stay is associated with poorer health outcomes and risk of nosocomial infections, amongst others.

Objective: To asses factors associated with inpatient endoscopy delays and impact on length of stay and 30-day readmission

Study design: Single center retrospective cohort study of all inpatient endoscopy procedures (gastroscopy, colonoscopy, ERCP, sigmoidoscopy) during 2016-2022. Data will be identified and extracted using CTCue. Only pseudonymized data will be used. Inpatient endoscopy delay will be defined as the number of days between the planned date versus the actual date. Multivariable logistic regression models will be performed to assess factors associated with inpatient endoscopy delay.

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Conditions studied

  • Inpatient Endoscopy Delay
  • Readmission
  • Prolonged Hospital Stay
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In context

Lead sponsor

Radboud University Medical Center is the lead sponsor of 959 studies on the registry; 134 are open to participants now.

Of its 6 completed or terminated interventional studies of FDA-regulated products, 0 (0%) have results posted.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Adult inpatients from all hospital departments undergoing endoscopy procedures. Patients will be selected via CTCue, with an admission based query that selects all adult patients with an admission of at least two days between 1-1-2014 and 1-12-2022 AND an endoscopic care activity.

Inclusion criteria

  • Adult patients (>18 years)
  • Clinical admission in any hospital department of at least two days during 1 January 2016 and 1 December 2022
  • Endoscopic procedure during clinical admission, including gastroscopy, endoscopic retrograde cholangiopancreatography (ERCP), endoscopic ultrasound (EUS), flexible sigmoidoscopy, colonoscopy

Exclusion criteria

Exclusion Criteria:

  • Elective admission
  • Procedure only for insertion of nasogastric or nasojejunal (feeding) tube without any other diagnostic or therapeutic aims
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Study design

Observational model
Cohort
Time perspective
Retrospective
Enrollment
3,700 participants (estimated)
Patient registry
No

Interventions

  • ProcedureInpatient gastrointestinal endoscopy

    all inpatient endoscopy procedures (gastroscopy, colonoscopy, ERCP, sigmoidoscopy) during 2016-2022.

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What researchers measure

Primary outcomes

  1. Rate of inpatient endoscopy delays (IED)

    IED will be defined as the number of days between the planned date versus the actual date.

    Time frame: at endoscopic procedure

  2. Difference in type of endoscopic procedure between patients with and without IED

    Type of endoscopic procedure: gastroscopy/colonoscopy/endoscopic retrograde cholangio-pancreaticography (ERCP)

    Time frame: at endoscopic procedure

  3. Difference in type of sedation between patients with and without IED

    Type of sedation during endoscopic procedure: No sedation/conscious sedation/general anesthesia

    Time frame: at endoscopic procedure

Secondary outcomes

  1. Median length of hospital stay

    length of hospital admission in days

    Time frame: through study cohort period from 1 january 2016 until 31 december 2022

  2. rate of 30-day readmissions

    percentage of readmissions within 30 days after initial discharge

    Time frame: up to 30 days

  3. Odds ratio of presence of inpatient endoscopy delays for risk of prolonged length of hospital stay and 30-day readmissions

    multivariable logistic regression modelling to assess factors associated with both outcomes and the impact of inpatient endoscopy delay

    Time frame: from admission till 30 days after discharge

  4. Odds ratio of presence of inpatient endoscopy delays for risk of 30-day readmissions

    multivariable logistic regression modelling to assess factors associated with both outcomes and the impact of inpatient endoscopy delay

    Time frame: from admission till 30 days after discharge

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Study locations

1 site
  • Radboud university medical center
    Nijmegen, Gelderland 6525GA, Netherlands
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References and documents

Individual participant data

Plan to share: Yes — IPD will be shared upon reasonable request

Supporting information: Study protocol, Sap, Csr, Analytic code

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Nov 21, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT05798065
Lead sponsor
Radboud University Medical Center
Responsible party
Sponsor
First posted
Apr 4, 2023
Start date
Apr 1, 2025 (estimated)
Primary completion
Jun 30, 2025 (estimated)
Completion
Jun 30, 2025 (estimated)
Last update
Nov 21, 2024

Study contacts

Milou van Riswijk, MD, Msc
Contact
milou.vanriswijk@radboudumc.nl
+31615280185
Peter Siersema, MD, PhD
principal investigator · Radboud University Medical Center

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Nov 2024. You cannot join it, but the record below documents what was studied.

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