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

Completed

• Conditions: Cardiac Output, Low; High Blood Pressure

• Registration Number: NCT02852941
• Lead Sponsor: Medical University of Warsaw

Brief Summary

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.

Detailed Description

Not available

Study Timeline

• Study Start: 2016-07
• Study First Submitted: 2016-07-27
• Primary Completion: 2016-08
• Study Completion: 2016-08
• Study First Submitted QC: 2016-08-01
• Study First Posted: 2016-08-02
• Status Verified: 2016-09
• Last Update Submitted: 2016-09-12
• Last Update Posted: 2016-09-13

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 80

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

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Assessment of cardiac index in Stable Renal Transplant Recipients	1 day	Measurement of cardiac index (l/min/m2)

Secondary Outcome Measures

Name	Time	Method
Assessment of Systemic Vascular Resistance Index in Stable Renal Transplant Recipients	1 day	Measurement of Systemic Vascular Resistance Index (dynes-sec/cm-5/m2)
Assessment of Nutritional Status in Stable Renal Transplant Recipients	1 day	Measurement of amount of fat tissue (%)

Trial Locations

Locations (1)

Medical University of Warsaw; 🇵🇱 Warsaw, Mazovian, Poland