Additional identifiers
EudraCT number
ClinicalTrials.gov number
Protocol/serial number
N0084118518
Study information
Scientific title
Prospective randomised study of the effect of two levels of hemodilution during cardiopulmonary bypass on postoperative renal function
Acronym
Study hypothesis
To assess whether or not thinning the blood during surgery reduces the likelihood of kidney problems.
Ethics approval
Not provided at time of registration
Study design
Randomised controlled trial
Primary study design
Interventional
Secondary study design
Randomised controlled trial
Trial setting
Hospitals
Trial type
Treatment
Patient information sheet
Condition
Cardiovascular: Cardiopulmonary bypass
Intervention
Hemodilution 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 type
Procedure/Surgery
Phase
Drug names
Primary outcome measure
Not provided at time of registration
Secondary outcome measures
Not provided at time of registration
Overall trial start date
06/12/2002
Overall trial end date
01/01/2005
Reason abandoned (if study stopped)
Eligibility
Participant inclusion criteria
Not provided at time of registration
Participant type
Patient
Age group
Not Specified
Gender
Not Specified
Target number of participants
60 patients
Participant exclusion criteria
Not provided at time of registration
Recruitment start date
06/12/2002
Recruitment end date
01/01/2005
Locations
Countries of recruitment
United Kingdom
Trial participating centre
Castle Hill Hospital
Cottingham
HU16 5JQ
United Kingdom
Sponsor information
Organisation
Department of Health (UK)
Sponsor details
Richmond House
79 Whitehall
London
SW1A 2NL
United Kingdom
Sponsor type
Government
Website
Funders
Funder type
Research organisation
Funder name
The North and South Bank Research and Development Consortium (UK)
Alternative name(s)
Funding Body Type
Funding Body Subtype
Location
Results and Publications
Publication and dissemination plan
Not provided at time of registration
Intention to publish date
Participant level data
Not provided at time of registration
Basic results (scientific)
Publication list