Skip to main content
OpenTrials
Not Yet Recruiting

NCT Number: NCT05798065

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

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

Not Yet Recruiting

Trial opening soon.

Get Notified

Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Radboud university medical center

Nijmegen, Gelderland, 6525GA, Netherlands

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

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

Treatment and study plan

Inpatient gastrointestinal endoscopy

Procedure

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

Primary outcomes

  1. Rate of inpatient endoscopy delays (IED)

    Time frame: at endoscopic procedure

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

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

    Time frame: at endoscopic procedure

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

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

    Time frame: at endoscopic procedure

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

Secondary outcomes

  1. Median length of hospital stay

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

    length of hospital admission in days

  2. rate of 30-day readmissions

    Time frame: up to 30 days

    percentage of readmissions within 30 days after initial discharge

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

    Time frame: from admission till 30 days after discharge

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

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

    Time frame: from admission till 30 days after discharge

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

Study contacts

Contact information is provided by the study sponsor or research team.

Milou van Riswijk, MD, Msc

CONTACT

[email protected]

+31615280185

Sponsors and collaborators

Lead sponsor

Radboud University Medical Center

Other

Registry information

Acronym: Impatience

Important dates

Study start
2025
Primary completion
2025
Study completion
2025
First posted
Apr 4, 2023
Registry last updated
Nov 21, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.