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Evaluation of Plasma Renin Concentrations in Cardiac Surgery

Evaluation of Plasma Renin Concentrations in Cardiac Surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06895213
Enrollment
100
Registered
2025-03-26
Start date
2025-04-14
Completion date
2026-12-01
Last updated
2026-08-10

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

Conditions

Cardiac Surgery With Cardiopulmonary Bypass

Keywords

renin-angiotensin system, RAS, hypotension, perfusion, shock, blood pressure

Brief summary

The purpose of this research is to learn more about how renin (a blood test) is affected by cardiopulmonary bypass, the heart-lung machine used during open heart surgery. Renin is a protein that may be elevated in response to low blood pressure or situations where organs do not receive sufficient oxygen. Renin may potentially be used as an indicator for specific treatments aimed to increase the blood pressure. This study will evaluate blood samples for renin concentration throughout the course of open heart surgery.

Detailed description

The investigator hypothesizes that renin concentrations will increase with exposure to cardiopulmonary bypass and that increased renin concentrations will be associated with the development of vasoplegia. Specific Aim 1. To characterize the effects of cardiopulmonary bypass on plasma renin concentrations in adults undergoing cardiac surgery. Specific Aim 2. To test the prognostic value of plasma renin concentrations on outcomes following cardiac surgery.

Interventions

None listed

Sponsors

Mayo Clinic
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Adult persons 18 years of age or greater. * Scheduled for an elective cardiac surgical procedure involving the use of cardiopulmonary bypass.

Exclusion criteria

* Surgery involving heart or lung transplantation or implant of a durable left ventricular assist device. * Emergency cardiac surgery. * Established diagnosis of any congenital heart disease. * End-stage kidney disease receiving kidney replacement therapy before surgery.

Design outcomes

Primary

MeasureTime frame
Plasma renin concentrationsUp to 24 hours after surgery

Secondary

MeasureTime frameDescription
VasoplegiaFirst 24 hours postoperativeRequirement of any vasopressor to maintain a mean arterial pressure of 65 mmHg or greater despite a cardiac index of at least 2.2 L/min/m2 with or without the need for pharmacologic inotropy
Acute kidney injury7 daysAssessed by the Kidney Disease Improving Global Outcomes (KDIGO) staging criteria
Organ dysfunction28 daysThe presence of any organ support therapy including vasopressors, renal replacement therapy, and mechanical ventilation
Mortality28 days

Countries

United States

Contacts

PRINCIPAL_INVESTIGATORPatrick M Wieruszewski, Pharm.D.

Mayo Clinic

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 11, 2026