Investigations Into Sepsis-associated Acute Kidney Injury

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-100
SponsorUniversity Hospital of North Norway

About this trial

In this study the investigators would like to study systemic and regional disturbances in patients with sepsis-associated acute kidney injury and in healthy controls undergoing laparoscopic abdominal surgery. Specifically study metabolic, hemodynamic and oxygen transport variables.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Sepsis diagnosed or suspected

Normal premorbid serum creatinine measured or anticipated (if data are not available)

Normovolemia as indicated by a pulse pressure variation less than 12%

Previously healthy individuals scheduled for laparoscopic colon cancer resection

Disqualifiers

None

Trial population

Intensiv care patients Surgical patients

Trial design

Design model

Case-control

Time perspective

Prospective

Treatments tested in this trial

  • Para Aminohippurate

    Drug

    Measurements of renal plasma flow and glomerular filtration rate

Treatment groups

20 Participants
are divided into 2 treatment groups
Group A: Sepsis patients1 intervention
Group B: Surgical patients1 intervention

Trial outcomes

Primary outcomes

1

Hemodynamics

Systemic and regional hemodynamics

Time frame
Repeated measures at 10am, 12am, 2pm, 4pm,6pm, and 8pm

Secondary outcomes

1

Metabolic alterations

Renal arginine metabolism

Time frame
Repeated measures at 10am, 12am, 2pm, 4pm,6pm, and 8pm

Other outcomes

Sponsors and contacts

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