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Patient Preference for Radial Versus Femoral Vascular Access (PREVAS)

T

Thorax Centrum Twente

Status

Completed

Conditions

Coronary Artery Disease

Treatments

Other: Questionnaire

Study type

Observational

Funder types

Other

Identifiers

NCT02625493
Prevas-v2

Details and patient eligibility

About

The purpose of this study is to determine the preference of patients regarding the vascular access site in future coronary procedures. We hypothesize that patients prefer the lesser invasive procedure via radial access.

Full description

Rationale: To explore patient preference for vascular access site in percutaneous coronary procedures, by assessing the perceived importance of benefits and risks of both transradial access and transfemoral access. In addition, direct preference for vascular access and preference for shared decision-making were evaluated.

Objective: To investigate the patient preference of vascular access -transradial versus transfemoral- in future percutaneous coronary procedures, by use of the Best-Worst Scaling.

Study design: Single-center, prospective, observational registry

Study population: A consecutive series of patients, who between June and August 2014, underwent elective coronary procedures at Thoraxcentrum Twente in Enschede.

Intervention: All subjects will receive a questionnaire containing basic baseline questions and a best-worst scaling scenario in which they were asked to indicate the most and least desirable characteristics of the vascular access approach.

Furthermore, their direct preference was asked and to which extent they preferred to participate in the decision-making process regarding the choice for vascular access route in future percutaneous coronary procedures.

Main study endpoints:

  • The primary endpoint is the patient preference on specific treatment characteristics with regard to vascular access in coronary procedures.

  • Secondary endpoints include

    1. direct patient preference for transradial access or transfemoral access
    2. the valuation of participation in decision-making on the choice of vascular access together with the interventional cardiologist.

Enrollment

198 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • All patients who undergoing an elective coronary procedure at Thoraxcenteum Twente in the period of June 2014 until August 2014

Exclusion criteria

  • Language barrier

Trial design

198 participants in 1 patient group

study population
Description:
All patients who underwent elective coronary procedures belonged to the one group, they received standard care without any additional interventions, but were asked to fill in a questionnaire.
Treatment:
Other: Questionnaire

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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