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Personalized Mean Arterial Pressure Management on Renal Function During Septic Shock (DORESEP)

Primary Purpose

Septic Shock, Acute Kidney Injury

Status
Completed
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
Haemodynamic management
Haemodynamic management
Sponsored by
Assistance Publique - Hôpitaux de Paris
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Septic Shock focused on measuring Sepsis, Acute kidney injury, Mean arterial pressure, Catecholamines, Renal doppler

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Any patient with septic shock may be included in the next 6 to 16h
  • Age > 18 years old and <= 80 years

Exclusion Criteria:

  • Chronic renal failure (Baseline serum creatinine > 120 mmol/L)
  • Chronic cardiac failure (Left ventricle ejection fraction < 40%)
  • Pregnancy
  • Urinary Tract Infection
  • Patients with a left ventricular dysfunction ( ventricular ejection fraction <40%)

Sites / Locations

  • Reanimation Chirurgicale - Hôpital Kremlin Bicêtre

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Test group

Control group

Arm Description

Patients will be treated with fluid and norepinephrine to achieve and maintain a mean arterial pressure of 65 mm Hg. Then they will be randomized in two groups. In the first group (study group, n=30), mean arterial pressure will be increased to 85 mm Hg for 72 hours by increasing the dose of norepinephrine in patients (A maximum dose of 1.2 mcg / kg / min is not exceeded). Key details, e.g., for drugs include dosage form, dosage, frequency and duration.

Patients will be treated with fluid and norepinephrine to achieve and maintain a mean arterial pressure of 65 mm Hg. Then they will be randomized in two groups. In this group (control group, n=30), mean arterial pressure will be maintained at 65 mm Hg.

Outcomes

Primary Outcome Measures

Acute kidney injury according to RIFLE score

Secondary Outcome Measures

Need for renal replacement therapy
including metabolic indications (Azotemia Serum urea ≥ 36mmol/L (100 mg/dL) ; Uremic complications : encephalopathy, pericarditis, bleeding ; Hyperkalemia K+ ≥ 6 mmol/L and/or electrocardiogram abnormalities ; Hypermagnesemia ≥4 mmol/L and/or anuria/absent deep tendon reflexes ; Acidosis Serum pH ≤ 7.15), Oligo-anuria Urine output <200mL/12 h or anuria, Fluid overload like Diuretic-resistant organ edema in the presence of acute kidney injury.
All cause mortality
All Cause mortality at 28 days, including refractory shock, refractory hypoxia, multiple organ failure, decisions to forgo life-sustaining therapies (DFLSTs)

Full Information

First Posted
October 14, 2011
Last Updated
January 8, 2020
Sponsor
Assistance Publique - Hôpitaux de Paris
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1. Study Identification

Unique Protocol Identification Number
NCT01473498
Brief Title
Personalized Mean Arterial Pressure Management on Renal Function During Septic Shock
Acronym
DORESEP
Official Title
Personalized Haemodynamic Management of Septic Shock: Influence of Mean Arterial Pressure Level on Renal Function: Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
January 2020
Overall Recruitment Status
Completed
Study Start Date
January 2013 (undefined)
Primary Completion Date
October 2015 (Actual)
Study Completion Date
November 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Assistance Publique - Hôpitaux de Paris

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Sepsis is the most severe complication of infections. Sepsis-associated Acute kidney injury (AKI) is commonly encountered in critically ill patients and independently predicts poor outcome. Unfortunately, no drug or management strategy was able to reduce incidence of AKI. To adapt the level of mean arterial pressure according to local renal hemodynamic evaluated by renal Doppler could lead to a better renal perfusion, and then less AKI.
Detailed Description
Acute Kidney Injury (AKI) is a frequent and serious complication of sepsis. Renal ischemia plays a major role in the pathophysiology of sepsis-associated AKI. There is currently no treatment to prevent or to treat AKI. It has been shown that a resistivity index (RI) greater than 0.74 of patients with septic shock could predict the occurrence of renal failure, and that increase mean arterial pressure (MAP) with norepinephrine could decrease RI. Hence, we propose to compare the frequency and the severity of the sepsis-associated AKI according to the early hemodynamic management of septic shock. Patients will be randomized in a classic group (MAP 65 mmHg) and an interventional group (MAP 85 mmHg). We can thus determine whether the level of MAP influences renal function, and whether this influence of MAP is dependent of renal perfusion assessed by renal Doppler. Participants will be followed for the duration of hospital stay, an expected average of 4 weeks. Primary endpoint: -Presence and severity of sepsis-associated AKI at day 7. Secondary endpoints: Acute renal failure measured by Classification AKI at day 28. Acute renal failure as measured by the RIFLE classification in the fourth to seventh day and 28th day. Use of renal replacement therapy during hospitalization in intensive care unit Mortality at day 28 Duration of study: Recruitment: 10 months, the patient monitoring: 28 days ± 3 days, total test duration: 11 months

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Septic Shock, Acute Kidney Injury
Keywords
Sepsis, Acute kidney injury, Mean arterial pressure, Catecholamines, Renal doppler

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
27 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Test group
Arm Type
Experimental
Arm Description
Patients will be treated with fluid and norepinephrine to achieve and maintain a mean arterial pressure of 65 mm Hg. Then they will be randomized in two groups. In the first group (study group, n=30), mean arterial pressure will be increased to 85 mm Hg for 72 hours by increasing the dose of norepinephrine in patients (A maximum dose of 1.2 mcg / kg / min is not exceeded). Key details, e.g., for drugs include dosage form, dosage, frequency and duration.
Arm Title
Control group
Arm Type
Active Comparator
Arm Description
Patients will be treated with fluid and norepinephrine to achieve and maintain a mean arterial pressure of 65 mm Hg. Then they will be randomized in two groups. In this group (control group, n=30), mean arterial pressure will be maintained at 65 mm Hg.
Intervention Type
Other
Intervention Name(s)
Haemodynamic management
Intervention Description
Patients will be treated with fluid and norepinephrine to achieve and maintain a mean arterial pressure of 65 mm Hg. Then they will be randomized in two groups. In the first group (study group, n=30), mean arterial pressure will be increased to 85 mm Hg for 72 hours by increasing the dose of norepinephrine in patients.
Intervention Type
Other
Intervention Name(s)
Haemodynamic management
Intervention Description
Patients will be treated with fluid and norepinephrine to achieve and maintain a mean arterial pressure of 65 mm Hg. Then they will be randomized in two groups. In this group (control group, n=30), mean arterial pressure will be maintained at 65 mm Hg.
Primary Outcome Measure Information:
Title
Acute kidney injury according to RIFLE score
Time Frame
at 7 days
Secondary Outcome Measure Information:
Title
Need for renal replacement therapy
Description
including metabolic indications (Azotemia Serum urea ≥ 36mmol/L (100 mg/dL) ; Uremic complications : encephalopathy, pericarditis, bleeding ; Hyperkalemia K+ ≥ 6 mmol/L and/or electrocardiogram abnormalities ; Hypermagnesemia ≥4 mmol/L and/or anuria/absent deep tendon reflexes ; Acidosis Serum pH ≤ 7.15), Oligo-anuria Urine output <200mL/12 h or anuria, Fluid overload like Diuretic-resistant organ edema in the presence of acute kidney injury.
Time Frame
during hospitalization
Title
All cause mortality
Description
All Cause mortality at 28 days, including refractory shock, refractory hypoxia, multiple organ failure, decisions to forgo life-sustaining therapies (DFLSTs)
Time Frame
at 28 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Any patient with septic shock may be included in the next 6 to 16h Age > 18 years old and <= 80 years Exclusion Criteria: Chronic renal failure (Baseline serum creatinine > 120 mmol/L) Chronic cardiac failure (Left ventricle ejection fraction < 40%) Pregnancy Urinary Tract Infection Patients with a left ventricular dysfunction ( ventricular ejection fraction <40%)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jacques DURANTEAU, MD,PhD
Organizational Affiliation
Assistance Publique - Hôpitaux de Paris
Official's Role
Principal Investigator
Facility Information:
Facility Name
Reanimation Chirurgicale - Hôpital Kremlin Bicêtre
City
Kremlin Bicêtre
ZIP/Postal Code
94275
Country
France

12. IPD Sharing Statement

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Personalized Mean Arterial Pressure Management on Renal Function During Septic Shock

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