Prospective randomised study of the effect of two levels of hemodilution during cardiopulmonary bypass on postoperative renal function

ISRCTN ISRCTN79851724
DOI https://doi.org/10.1186/ISRCTN79851724
Secondary identifying numbers N0084118518
Submission date
12/09/2003
Registration date
12/09/2003
Last edited
05/12/2014
Recruitment status
No longer recruiting
Overall study status
Completed
Condition category
Circulatory System
Prospectively registered
Protocol
Statistical analysis plan
Results
Individual participant data
Record updated in last year

Plain English summary of protocol

Not provided at time of registration

Contact information

Mr Levent Guvendik
Scientific

CardioThoracic Surgical Unit
Castle Hill Hospital
Castle Road
Cottingham
HU16 5JQ
United Kingdom

Study information

Study designRandomised controlled trial
Primary study designInterventional
Secondary study designRandomised controlled trial
Study setting(s)Hospital
Study typeTreatment
Scientific titleProspective randomised study of the effect of two levels of hemodilution during cardiopulmonary bypass on postoperative renal function
Study objectivesTo assess whether or not thinning the blood during surgery reduces the likelihood of kidney problems.
Ethics approval(s)Not provided at time of registration
Health condition(s) or problem(s) studiedCardiovascular: Cardiopulmonary bypass
InterventionHemodilution level 1 vs hemodilution level 2.

Five blood and urine samples will be taken: after anaesthesia but before surgery, at the end of the operation, 12 h after, 1 day after and 2 days after.
Intervention typeProcedure/Surgery
Primary outcome measureNot provided at time of registration
Secondary outcome measuresNot provided at time of registration
Overall study start date06/12/2002
Completion date01/01/2005

Eligibility

Participant type(s)Patient
Age groupNot Specified
SexNot Specified
Target number of participants60 patients
Key inclusion criteriaNot provided at time of registration
Key exclusion criteriaNot provided at time of registration
Date of first enrolment06/12/2002
Date of final enrolment01/01/2005

Locations

Countries of recruitment

  • England
  • United Kingdom

Study participating centre

Castle Hill Hospital
Cottingham
HU16 5JQ
United Kingdom

Sponsor information

Department of Health (UK)
Government

Richmond House
79 Whitehall
London
SW1A 2NL
United Kingdom

Website http://www.doh.gov.uk

Funders

Funder type

Research organisation

The North and South Bank Research and Development Consortium (UK)

No information available

Results and Publications

Intention to publish date
Individual participant data (IPD) Intention to shareNo
IPD sharing plan summaryNot provided at time of registration
Publication and dissemination planNot provided at time of registration
IPD sharing plan