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Clinician Decision Making Regarding Surveillance for Low-risk Intraductal Papillary Mucinous Neoplasms of The Pancreas

NYU Langone Health logo

NYU Langone Health

Status

Completed

Conditions

Surgery Risk Assessment

Study type

Observational

Funder types

Other

Identifiers

NCT06311032
22-01227

Details and patient eligibility

About

The main objective of this study is to determine how physicians make decisions regarding surveillance of Intraductal Papillary Mucinous Neoplasm's (IPMN) of the pancreas.

Full description

The study will employ a survey design that poses physicians with a series of three clinical case vignettes. Each vignette describes an IPMN of varying severity, and the physician will be asked determine whether they would continue or discontinue clinical surveillance in each case.

This will be a double-blinded randomized survey study, featuring two arms. Providers will be randomized to either be provided with, or not provided with a risk stratification tool (DART-1) when presented with their clinical case vignettes.

Enrollment

72 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Membership in either the PACYFIC or PRECEDE consortiums
  • Physician with expertise in the management of IPMN
  • Able and willing to complete survey

Exclusion criteria

  • Not a member of either the PACYFIC or PRECEDE consortiums
  • Not a physician with expertise in the management of IPMN

Trial design

72 participants in 2 patient groups

Vignettes with Risk Stratification Tool
Description:
Physicians will be posed with a series of three clinical case vignettes. Each vignette describes an IPMN of varying severity, and the physician will be asked determine whether they would continue or discontinue clinical surveillance in each case. Participants in this arm will be provided a risk stratification tool (DART-1) when presented with their clinical case vignettes. The DART-1 is a 5-question tool which calculates the probability (%) of IPMNs without worrisome features or high-risk stigmata at diagnosis.
Vignettes without Risk Stratification Tool
Description:
Physicians will be posed with a series of three clinical case vignettes. Each vignette describes an IPMN of varying severity, and the physician will be asked determine whether they would continue or discontinue clinical surveillance in each case. Participants in this arm will be not be provided a risk stratification tool when presented with their clinical case vignettes.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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