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

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

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN79851724
Enrollment
60
Registered
2003-09-12
Start date
2002-12-06
Completion date
Unknown
Last updated
2015-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cardiovascular: Cardiopulmonary bypass Circulatory System Cardiopulmonary bypass

Interventions

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.

Sponsors

Record provided by the NHS Trusts Clinical Trials Register - Department of Health (UK)
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Not provided at time of registration

Exclusion criteria

Exclusion criteria: Not provided at time of registration

Design outcomes

Primary

MeasureTime frame
Not provided at time of registration

Secondary

MeasureTime frame
Not provided at time of registration

Countries

United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026