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RECCORD (Recording Courses of Vascular Diseases) Registry

D

Deutsche Gesellschaft für Angiologie, Gesellschaft für Gefäßmedizin e.V.

Status

Enrolling

Conditions

Claudication
Diabetic Foot
Peripheral Artery Disease
Critical Limb Ischemia
Vascular Diseases

Study type

Observational

Funder types

Other

Identifiers

NCT03448029
U1111-1209-6562 (Other Identifier)
RECCORD
DRKS00013585 (Registry Identifier)

Details and patient eligibility

About

The RECording COurses of vasculaR Diseases registry (RECCORD registry) is an observational, prospective, multicentre, all-comers registry platform.

In the initial phase, patients referred for endovascular revascularization of peripheral artery disease (PAD) of the lower limbs will be prospectively included and followed up for at least one year.

At baseline, data on patients' demographic characteristics, comorbidities, previous peripheral interventions, medication, and clinical stage of PAD (Rutherford category), haemodynamic parameters, and procedural data including complications will be assessed.

Major adverse cardiac and limb events will be recorded at planned (at six and 12 months) and at any unplanned visits.

For details see NM Malyar et al., Rationale and design of the RECording COurses of vasculaR Diseases registry (RECCORD registry). Vasa. https://doi.org/10.1024/0301-1526/a000631

Full description

For details see NM Malyar et al., Rationale and design of the RECording COurses of vasculaR Diseases registry (RECCORD registry). Vasa.

https://doi.org/10.1024/0301-1526/a000631

Enrollment

6,000 estimated patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

  • any type of endovascular interventions for symptomatic PAD
  • endovascular intervention for PAD of lower extremities, i.e. below the aorto-iliac bifurcation

Exclusion criteria

  • patients undergoing hybrid-(surgical and endovascular) and/or surgical interventions for symptomatic PAD
  • patients with a life expectancy of <6 months
  • endovascular intervention for reasons other than symptomatic PAD

Trial design

6,000 participants in 1 patient group

Endovascular Patients
Description:
Patients undergoing endovascular interventions for symptomatic PAD

Trial contacts and locations

1

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Central trial contact

Nasser Malyar, Dr.; Ulrich Hoffmann, Prof.

Data sourced from clinicaltrials.gov

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