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OpenTrials
Completed

NCT Number: NCT02852941

Assessment of Volumetric Hemodynamic Parameters and Nutritional Status in Stable Renal Transplant Recipients

Changes in volumetric hemodynamic parameters and fluid overload (Cardiac Index,Stroke Volume, Thoracic Fluid Content, Systemic Vascular Resistance) were measured using a impedance cardiography (ICG) (CardioScreen 1000 - Haemodynamic Measurement System, Medis. Ilmenau) in stable renal transplant recipients Nutritional status was measured by Tanita 418 Monitor.

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Key information

Conditions

Cardiac Output, Low Cardiovascular Diseases Heart Diseases High Blood Pressure Hypertension Pathological Conditions, Signs and Symptoms Signs and Symptoms Vascular Diseases

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Medical University of Warsaw

Warsaw, Mazovian, 02-091, Poland

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • give voluntary consent to participate in the study
  • functioning graft longer than 3 months to 10 years
  • no clinical cardiovascular disease during the 6 months preceding entry
  • stable graft function- glomerular filtration rate > 30 ml/min/1.73 m2, creatinine concentration <2.5 mg/dl
  • medical staff (medical doctors, nurses)

Exclusion criteria

  • not meet the above criteria
  • episode of illness (for example: infection)
  • pregnancy

Treatment and study plan

CardioScreen 1000

Device

Haemodynamic Measurement System, Medis Impedance cardiography (ICG)

Tanita 418- Bioelectrical impedance analysis

Device

The device measured the size of total body water (TBW), fat mass (FM%), visceral fat%, fat free mass (FFM), and basal metabolic rate (BMR) (kcal).

Primary outcomes

  1. Assessment of cardiac index in Stable Renal Transplant Recipients

    Time frame: 1 day

    Measurement of cardiac index (l/min/m2)

Secondary outcomes

  1. Assessment of Nutritional Status in Stable Renal Transplant Recipients

    Time frame: 1 day

    Measurement of amount of fat tissue (%)

  2. Assessment of Systemic Vascular Resistance Index in Stable Renal Transplant Recipients

    Time frame: 1 day

    Measurement of Systemic Vascular Resistance Index (dynes-sec/cm-5/m2)

Sponsors and collaborators

Lead sponsor

Medical University of Warsaw

Other

Registry information

Important dates

Study start
2016
Primary completion
2016
Study completion
2016
First posted
Aug 2, 2016
Registry last updated
Sep 13, 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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