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CompletedNCT05797116Updated Nov 18, 2023

Practice Variation in Preoperative MDT Meetings

An observational study in Multidisciplinary Communication, Preoperative Care and Patient Care Team, sponsored by Rijnstate Hospital. Completed at 1 site in Netherlands. Per ClinicalTrials.gov, last updated 2023-11-18.

Sponsored by Rijnstate Hospital · Observational

Study type
Observational
Model
Case-only
Time perspective
Cross-sectional
Enrollment
54
Sex
All
01

Study summary

The goal of this observational survey study is to evaluate the current practice variations of preoperative multidisciplinary team meetings (MDT meetings) for high risk noncardiac surgical patients. The main questions it aims to answer are:

  • What is the current variation in Dutch hospitals in the practice of preoperative MDT meetings for high risk noncardiac surgical patients?
  • Which facilitators and barriers influence the implementation process of preoperative MDT meetings? Participants are anesthesiologists in Dutch hospitals who will be asked to fill in a one-time survey. One anesthesiologist per anesthesiology department will be asked to fill in the survey. The survey will take approximately 5 to 10 minutes to complete.
Read the detailed description

The number of patients with multiple comorbidities is significantly growing. Medical advances have made it possible to perform challenging surgical interventions to increase life expectancy. Yet, it is this group of patients that has a high risk of complications after a surgical intervention leading to a reduction in their quality of life and self-sustainability. Current European and Dutch guidelines recommend the implementation of preoperative multidisciplinary team (MDT) meetings for high risk noncardiac surgical patients. However, the evidence underlying the guideline recommendations is scarce. Furthermore, the implementation process of a well-functioning MDT meeting can be a challenge and may sometimes lead to no MDT meeting at all. And finally, the guidelines do not specify conditions by who or how the MDT meeting should be done, for example required attending specialties or specific subjects to be discussed. A broad practice variation in preoperative MDT meetings might thus be present and could be a complicating factor in the equal treatment of patients compliant to 'best practice'. The current survey will evaluate practice variation of preoperative MDT meetings for high risk noncardiac surgical patients in the Netherlands and assess possible facilitators and barriers in the implementation process.

02

Conditions studied

  • Multidisciplinary Communication
  • Preoperative Care
  • Patient Care Team

Keywords

  • multidisciplinary team meeting
  • high risk surgical patients
  • preoperative
03

In context

Lead sponsor

Rijnstate Hospital is the lead sponsor of 127 studies on the registry; 14 are open to participants now.

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

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Sampling method
Non-probability sample

Study population

The participants in this study are anesthesiologists in the Netherlands, preferably those in charge of preoperative screening. One anesthesiologist per anesthesiology department may be included.

Inclusion criteria

  • Currently working as anesthesiologist in a Dutch hospital

Exclusion criteria

Exclusion Criteria:

  • No informed consent
05

Study design

Observational model
Case-only
Time perspective
Cross-sectional
Enrollment
54 participants (actual)
Patient registry
No

Groups and cohorts

  • Anaesthesiologists in the Netherlands

    The participants in this study are anesthesiologists in the Netherlands, preferably those in charge of preoperative screening. One anesthesiologist per anesthesiology department may be included.

    Other: Survey

Interventions

  • OtherSurvey

    29-item Dutch survey about the implementation and practice variation of preoperative multidisciplinary team (MDT) meetings for high risk noncardiac surgical patients in the Netherlands.

06

What researchers measure

Primary outcomes

  1. Percentage of anaesthesia departments who employ preoperative multidisciplinary team (MDT) meetings for high risk noncardiac surgical patients in Dutch hospitals.

    Percentage of anaesthesia departments who employ preoperative multidisciplinary team (MDT) meetings in which an anaesthesiologist is present, for high risk noncardiac surgical patients in Dutch hospitals.

    Time frame: Baseline

Secondary outcomes

  1. Frequency of multidisciplinary team (MDT) meetings per month

    An approximate frequency of preoperative multidisciplinary team (MDT) meetings for high risk noncardiac surgical patients per month

    Time frame: Baseline

  2. Number of patients discussed per multidisciplinary team (MDT) meeting

    Number of patients discussed per multidisciplinary team (MDT) meeting (average)

    Time frame: Baseline

  3. Duration of multidisciplinary team (MDT) meeting in minutes

    Duration of multidisciplinary team (MDT) meeting in minutes (average)

    Time frame: baseline

07

Study locations

1 site
  • Rijnstate Hospital
    Nijmegen, Netherlands
08

References and documents

Individual participant data

Plan to share: Yes — Data will be made accessible on request after agreement has been received from the entire project group. The principal investigator will communicate data availability with researchers sending the requests.

Supporting information: Study protocol, Sap, Icf

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 18, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05797116
Lead sponsor
Rijnstate Hospital
Responsible party
Sponsor
First posted
Apr 4, 2023
Start date
Jan 31, 2023
Primary completion
Mar 31, 2023
Completion
May 31, 2023
Last update
Nov 18, 2023

Study contacts

Carine JM Doggen, PhD
principal investigator · Rijnstate Hospital
Benedikt Preckel, MD, PhD
principal investigator · Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)

Oversight

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

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This study is completed, as verified in Nov 2023. You cannot join it, but the record below documents what was studied.

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