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Noninvasive Perioperative Monitoring of Arterial Stiffness, Volume and Nutritional Status in Stable Renal Transplant Recipients

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ClinicalTrials.gov Identifier: NCT02908139
Recruitment Status : Recruiting
First Posted : September 20, 2016
Last Update Posted : June 15, 2017
Sponsor:
Information provided by (Responsible Party):
Łukasz Czyżewski, Medical University of Warsaw

Brief Summary:
Central blood pressure and pulse wave velocity were measured using a BR 102 Plus PWA device in perioperative time after kidney transplantation

Condition or disease Intervention/treatment
Arterial Calcification Aortic Stiffness High Blood Pressure Kidney Transplantation Device: BR-102 plus PWA Device: Tanita MC780 MA S

Study Type : Observational
Estimated Enrollment : 40 participants
Observational Model: Cohort
Time Perspective: Prospective
Official Title: Noninvasive Perioperative Monitoring of Arterial Stiffness, Volume and Nutritional Status in Stable Renal Transplant Recipients
Study Start Date : September 2016
Estimated Primary Completion Date : September 2017
Estimated Study Completion Date : September 2017

Resource links provided by the National Library of Medicine


Group/Cohort Intervention/treatment
Patients before kidney transplantation
The study included who had been admitted to the TransplantClinic before kidney transplantation
Device: BR-102 plus PWA
Monitoring of Arterial Stiffness and Central Aortic Pressure

Device: Tanita MC780 MA S
The device measured the size of total body water (TBW), Extra Cellular Water (ECW), Intra Cellular Water (ICW), fat mass (FM%), visceral fat%, fat free mass (FFM) and basal metabolic rate, (BMR) (kcal).




Primary Outcome Measures :
  1. Differences in pulse wave velocity [m/s] in short postoperative period. [ Time Frame: 3 days (one day before kidney transplantation and two days after kidney transplantation) ]
    Assessment will be performed one day before kidney transplantation and two days after kidney transplantation


Secondary Outcome Measures :
  1. Differences in central aortic pressure [mmHg] in short postoperative period. [ Time Frame: 3 days (one day before kidney transplantation and two days after kidney transplantation) ]
    Assessment will be performed one day before kidney transplantation and two days after kidney transplantation



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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
A total of 40 consecutive patients admitted to Transplant Centre to perform kidney transplantataion were included in this study.
Criteria

Inclusion Criteria:

  • give voluntary consent to participate in the study
  • no clinical cardiovascular disease during the 6 months preceding entry

Exclusion Criteria:

  • not meet the above criteria

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02908139


Contacts
Contact: Lukasz Czyzewski, PhD 696457655 ext 48 czyzewski_lukasz@wp.pl

Locations
Poland
Medical University of Warsaw Recruiting
Warsaw, Mazowian, Poland, 02-091
Contact: Lukasz Czyzewski, PhD    696457655 ext 48    czyzewski_lukasz@wp.pl   
Principal Investigator: Lukasz Czyzewski, PhD         
Sub-Investigator: Janusz Wyzgal, Professor, MD         
Sub-Investigator: Emilia Czyzewska, MSc         
Sub-Investigator: Agnieszka Pacek, Student         
Sub-Investigator: Aleksandra Tomaszek, MSc         
Sub-Investigator: Lukasz Szarpak, PhD         
Sponsors and Collaborators
Medical University of Warsaw