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Completed

NCT Number: NCT02299960

Measurement of Endothelial Function and Cardiac Output: New Methods

The main purpose of this study is to analyse test-retest-reliability of functional quantification of endothelial dysfunction through puls-amplitude-tonometry in patients with heart failure with preserved/reduced ejection fraction, pulmonary hypertension, arterial hypertension and diabetic nephropathy. In the same group, test-retest-reliability of circulating endothelial cells as well as test-retest reliability of non invasive cardiac output Monitoring will be observed and analysed.

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Key information

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Clinically stable for the last 4 weeks (not for HFrEF: 7 days)
  • Signed consent form

HFpEF:

  • Baseline-Echocardiography:
  • hospitalization <= 12 months with diagnosis heart failure and E/E' > 8 or E' < 8 cm/s or
  • BNP >= 100pg/ml or NT-proBNP >= 300pg/ml in the last 6 months or
  • LAVI > 28 ml/m² and E/E' > 8 or E' < 8cm/s or PAPsys > 40mmHg and E/E' > 8 or E' < 8 cm/s
  • Possibility to take part in cardiac stress test
  • Heart failure NYHA I-III
  • Sinus rhythm
  • Max. O2-uptake on exertion < 20ml/kgBW/min

HFrEF

  • HFrEF due to ischemic or non-ischemic reasons
  • NYHA I-III
  • Individually optimized and stable pharmacological therapy (including beta-blocker, ACE-Inhibitor, AT1-antagonist, aldosterone-antagonist)
  • EF <=45%, Simpson Biplan PH
  • NICE-Classification 2013 I/II
  • PAH >= 25 mmHg
  • Precapillary PAH: Wedge-pressure <= 15 mmHg, CO normal or low
  • Postcapillary PAH: Wedge-pressure >= 15 mmHg, CO normal or low

Diabetic nephropathy:

  • Diabetes mellitus Type 2 with oral or Insulin therapy and one or more of the following:
  • Diabetic nephropathy has been diagnosed before (anamnesis)
  • Macroalbuminuria: Urine Albumine/Creatinine-ratio > 300mg/g Creatinine (>34mg/mmol) in 2 out of 3 tests of Urine in the morning and GFR <90ml/min/1.73m² (CKD-EPI)
  • Microalbuminuria: 30-300mg/g Creatinine (>=3.4 mg/mmol but <34mg/mmol) tested as above and GFR < 90 ml/min/1.73m² and diabetic retinopathy

AH:

  • Hypertension diagnosed at least 6 months except structural heart disease: EF > 55% and no sign of HFpEF
  • No symptoms of coronary heart disease
  • Possibility to take part in cardiac stress test
  • Stable pharmacologic therapy of Hypertension for at least 4 weeks
  • Systolic blood pressure <140 mmHG during Screening

Exclusion criteria

  • Patient incapable of contracting
  • Angina pectoris > CCS II
  • Coronary Intervention in the last 4 weeks or scheduled Intervention/Bypass
  • Myocardial infarction in the last 3 months
  • Stroke in the last 3 months
  • Valvular heart disease > II°
  • Cardiomyopathy due to Infiltrate/hypertrophic obstruction (e.g. HOCM, Amyloidosis)
  • Congenital complex heart disease
  • Active myocarditis
  • Significant lung disease
  • Significant Cardiac dysrhythmia
  • Scheduled changes in medication during time of study
  • (Scheduled) heart transplant
  • Cardiac resynchronisation therapy over the last three months
  • ICD/Pacemaker-implant in the last 4 weeks
  • Uncontrolled Hyper/Hypotension (>180mmHg, <95mmHg)
  • Patient taking part in Rehabilitation program
  • Diagnosed Malignant disease or disease with life expectancy < 1 year
  • Anemia with Hb<10mg/dl
  • Untreated significant thyroid disease

HFpEF, Hypertension and PH:

  • Patient incapable of cardiac stress test (e.g. because of orthopedic Problems)
  • Significant changes in cardiovascular Status over the two weeks of study
  • Instable cardiopulmonary Status over the last four weeks

HFrEF:

  • I.v. Treatment with inotropic drug or diuretic in the last 7 days before Screening
  • Myocardial infarction in the last 4 weeks

Treatment and study plan

Endo-PAT

Device

Analysis of endothelial function through pulse-amplitude-tonometry

NICOM

Device

Non-invasive measurement of cardiac output

Primary outcomes

  1. Test-retest-reliability EndoPAT

    Time frame: 2 weeks

Secondary outcomes

  1. Test-retest-reliability circulating endothelial cells

    Time frame: 2 weeks

  2. Test-retest-reliability NICOM

    Time frame: 2 weeks

  3. Correlation: Cardiac Output on exertion and cardiopulmonary exercise test and 6 Minute Walking test

    Time frame: 2 weeks

  4. Correlation: circulating endothelial cells and EndoPAT and endothelial function

    Time frame: 2 weeks

    will include the molecular diagnostic of circulating endothelial cells

  5. Variability of biomarkers of myocardiac remodelling and of cardiorenal syndrome

    Time frame: 2 weeks

  6. Correlation cardiac Output on exertion and echocardiography in HFpEF

    Time frame: 2 weeks

  7. Clinical feasibility of circulating endothelial cells and EndoPAT

    Time frame: 2 weeks

Sponsors and collaborators

Lead sponsor

Charite University, Berlin, Germany

Other

Collaborators

  • Bayer
  • Health Twist GmbH

Registry information

Official study title

Pilot Study: Analysis of Endothelial Function Through Circulating Endothelial Cells and Puls-amplitude-tonometry and of Non-invasive Measurement of Cardiac Output on Exertion in Patients With Heart Failure, Pulmonary Hypertension, Arterial Hypertension and Diabetic Nephropathy

Important dates

Study start
2014
Primary completion
2015
Study completion
2015
First posted
Nov 24, 2014
Registry last updated
Jun 10, 2016

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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