Coronary Artery Disease and Renal Failure Registry

NCT ID: NCT00679419

Last Updated: 2012-11-02

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

UNKNOWN

Total Enrollment

3352 participants

Study Classification

OBSERVATIONAL

Study Start Date

2007-12-31

Study Completion Date

2013-05-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

It is the aim of the multi-centric and prospective registry to analyze in patients with CAD the impact of different grades of renal failure on the outcome and course of the patients and to correlate these with clinical variables.

In particular, the registry has the following objectives:

* prospective consecutive assessment of all patients with coronary artery disease and renal failure in the participating hospitals of the registry
* evaluation of the outcome and course of patients with regard to their different stages of renal failure at baseline
* analysis of the impact of different therapeutic strategies on acute and long-term outcomes
* identification of clinical risk factors, novel biomarkers and genetic markers for an unfavorable long-term outcome

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Coronary Artery Disease Renal Failure

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Group 0 (Controllgroup)

eGFR \>= 90 ml/min/1.73m\^2 and no proteinuria

No interventions assigned to this group

Group 1

eGFR \>= 90 ml/min/1.73m\^2 and proteinuria

No interventions assigned to this group

Group 2

eGFR 60 - 89 ml/min/1.73m\^2

No interventions assigned to this group

Group 3

eGFR 30 - 59 ml/min/1.73m\^2

No interventions assigned to this group

Group 4

eGFR 15 - 29 ml/min/1.73m\^2

No interventions assigned to this group

Group 5

eGFR \< 15 ml/min/1.73m\^2 or requiring dialysis

No interventions assigned to this group

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Women and men \>= 18 years of age
* Patients with actually performed interventional coronary angiography and there a documented coronary heart disease, defined as at least one documented stenosis \>= 50 % in at least one main coronary vessel (Main steam; RCX; RIVA; RCA)
* European/Caucasian descent (European/Caucasian parents and grandparents)
* Availability of an urine, serum- and EDTA blood sample of the patient
* Documented consent of patients for handling of personal medical data, including a genetic analysis

Exclusion Criteria

* Patients who have been already recruited into this registry
* Patients with organ transplantations, apart from kidney transplantations
* Immunosuppressive therapy, apart from immunosuppressive therapy after kidney transplantation
* Patients with polycystic renal disease
* Pregnant and breastfeeding patients
* Known malignant tumor
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

BMBf (Federal Ministry of Education and Research)

UNKNOWN

Sponsor Role collaborator

KfH Kuratorium für Dialyse und Nierentransplantation e.V.

UNKNOWN

Sponsor Role collaborator

Amgen

INDUSTRY

Sponsor Role collaborator

AstraZeneca

INDUSTRY

Sponsor Role collaborator

Boehringer Ingelheim

INDUSTRY

Sponsor Role collaborator

Sanofi

INDUSTRY

Sponsor Role collaborator

Institut für Klinisch-Kardiovaskuläre Forschung GmbH

NETWORK

Sponsor Role lead

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Eva Brand, Prof. Dr.

Role: PRINCIPAL_INVESTIGATOR

University Hospital of Muenster

Holger Reinecke, Prof. Dr.

Role: PRINCIPAL_INVESTIGATOR

University Hospital of Muenster

Günter Breithardt, Prof. Dr.

Role: PRINCIPAL_INVESTIGATOR

University Hospital of Muenster

Hermann Pavenstädt, Prof. Dr.

Role: PRINCIPAL_INVESTIGATOR

University Hospital of Muenster

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Universitätsklinikum Aachen

Aachen, , Germany

Site Status

Zentralklinik Bad Berka

Bad Berka, , Germany

Site Status

Herz- und Gefäßklinik Bad Neustadt

Bad Neustadt an der Saale, , Germany

Site Status

Schüchtermann-Klinik

Bad Rothenfelde, , Germany

Site Status

Herzzentrum Brandenburg

Brandenburg, , Germany

Site Status

St.-Vincenz-Hospital

Coesfeld, , Germany

Site Status

Klinikum Lippe-Detmold

Detmold, , Germany

Site Status

Herzzentrum Duisburg

Duisburg, , Germany

Site Status

Evangelisches Krankenhaus Düsseldorf

Düsseldorf, , Germany

Site Status

Alfried Krupp Krankenhaus Essen

Essen, , Germany

Site Status

Klinikum Garmisch-Partenkirchen

Garmisch-Partenkirchen, , Germany

Site Status

Universitätsklinikum Halle/Saale

Halle, , Germany

Site Status

Universitätsklinikum Hamburg-Eppendorf

Hamburg, , Germany

Site Status

Evangelisches Krankenhaus Hamm

Hamm, , Germany

Site Status

St. Marienhospital Hamm

Hamm, , Germany

Site Status

Medizinische Hochschule Hannover

Hanover, , Germany

Site Status

SLK-Kliniken Heilbronn GmbH

Heilbronn, , Germany

Site Status

Privatklinik Dr. Schindlbeck

Herrsching am Ammersee, , Germany

Site Status

Herzzentrum Lahr

Lahr, , Germany

Site Status

Kardiologische Praxis Dr. Schön

Mühldorf, , Germany

Site Status

Klinik Augustium München

München, , Germany

Site Status

Klinikum Neuperlach

München, , Germany

Site Status

Raphaelsklinik Münster

Münster, , Germany

Site Status

St. Franziskus-Hospital

Münster, , Germany

Site Status

Universitätsklinikum Münster

Münster, , Germany

Site Status

Lukaskrankenhaus Neuss

Neuss, , Germany

Site Status

Euregioclinic Nordhorn

Nordhorn, , Germany

Site Status

St. Vincenz-Krankenhaus

Paderborn, , Germany

Site Status

Klinikum Pirna

Pirna, , Germany

Site Status

Christliches Krankenhaus Quakenbrück e.V.

Quakenbrück, , Germany

Site Status

Zentralklinikum Suhl

Suhl, , Germany

Site Status

Josephs-Hospital Warendorf

Warendorf, , Germany

Site Status

Countries

Review the countries where the study has at least one active or historical site.

Germany

References

Explore related publications, articles, or registry entries linked to this study.

Engelbertz C, Pinnschmidt HO, Freisinger E, Reinecke H, Schmitz B, Fobker M, Schmieder RE, Wegscheider K, Breithardt G, Pavenstadt H, Brand E. Sex-specific differences and long-term outcome of patients with coronary artery disease and chronic kidney disease: the Coronary Artery Disease and Renal Failure (CAD-REF) Registry. Clin Res Cardiol. 2021 Oct;110(10):1625-1636. doi: 10.1007/s00392-021-01864-5. Epub 2021 May 26.

Reference Type DERIVED
PMID: 34036426 (View on PubMed)

Engelbertz C, Reinecke H, Breithardt G, Schmieder RE, Fobker M, Fischer D, Schmitz B, Pinnschmidt HO, Wegscheider K, Pavenstadt H, Brand E. Two-year outcome and risk factors for mortality in patients with coronary artery disease and renal failure: The prospective, observational CAD-REF Registry. Int J Cardiol. 2017 Sep 15;243:65-72. doi: 10.1016/j.ijcard.2017.05.022. Epub 2017 May 7.

Reference Type DERIVED
PMID: 28526542 (View on PubMed)

Brand E, Pavenstadt H, Schmieder RE, Engelbertz C, Fobker M, Pinnschmidt HO, Wegscheider K, Breithardt G, Reinecke H. The Coronary Artery Disease and Renal Failure (CAD-REF) registry: trial design, methods, and aims. Am Heart J. 2013 Sep;166(3):449-56. doi: 10.1016/j.ahj.2013.06.010. Epub 2013 Jul 23.

Reference Type DERIVED
PMID: 24016493 (View on PubMed)

Related Links

Access external resources that provide additional context or updates about the study.

http://cadref.de

CAD-REF Homepage

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

1-071812

Identifier Type: -

Identifier Source: org_study_id