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Transferability and Cost-effectiveness of PROSPECT in Surgical Trainees

NCT01965860 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 39

Last updated 2021-03-16

Study results available
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Summary

To design, validate and prove cost-effectiveness of a comprehensive endovascular simulation curriculum consisting of cognitive and psychomotor skills training for endovascular management of symptomatic vascular disease in the lower limbs.

Conditions

  • Vascular Disease

Interventions

OTHER

additional curriculum (E-learning + simulation)

OTHER

additional E-learning

Sponsors & Collaborators

  • University Ghent

    lead OTHER

Principal Investigators

  • Isabelle Van Herzeele, MD, PhD · University Ghent

Study Design

Allocation
RANDOMIZED
Purpose
HEALTH_SERVICES_RESEARCH
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2014-08-31
Primary Completion
2016-02-29
Completion
2016-02-29

Countries

  • Belgium

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01965860 on ClinicalTrials.gov