Peripheral Perfusion Versus Lactate Targeted Fluid Resuscitation in Septic Shock
1 other identifier
interventional
46
1 country
1
Brief Summary
Persistent hyperlactatemia has been traditionally considered as representing tissue hypoxia, and lactate normalization is recommended as a resuscitation target by the Surviving Sepsis Campaign (SSC). However, other sources contribute to hyperlactatemia such as sustained adrenergic activity and impaired lactate clearance. Only hypoperfusion-related hyperlactatemia might be reversed by optimizing systemic blood flow. Fluid resuscitation (FR) is used to improve cardiac output (CO) in septic shock to correct hypoperfusion. Nevertheless, if persistent hyperlactatemia is not hypoxia-related, excessive FR could lead to flow overload. In addition, kinetics of recovery of lactate is relatively slow, and thus it might be a suboptimal target for FR. Peripheral perfusion appears as a promising alternative target. Abnormal capillary refill time (CRT) is frequently used as trigger for FR in septic shock. Studies demonstrated the strong prognostic value of persistent abnormal peripheral perfusion, and some recent data suggest that targeting FR on CRT normalization could be associated with less fluid loading and organ dysfunctions. The excellent prognosis associated with CRT recovery, the rapid-response time to fluid loading, its simplicity, and its availability in resource-limited settings, constitute a strong background to promote studies evaluating its usefulness to guide FR . The study hypothesis is that a CRT-targeted FR is associated with less positive fluid balances, organ dysfunctions, and at least similar improvement of tissue hypoperfusion or hypoxia, when compared to a lactate-targeted FR. To test this hypothesis, the investigators designed a clinical physiological, randomized controlled trial in septic shock patients. Recruited patients will be randomized to FR aimed at normalizing CRT or normalizing or decreasing lactate \>20% every 2 h during the study period. Fluid challenges (500 ml in 30 min intervals) will be repeated until perfusion target is achieved, or dynamic predictors of fluid responsiveness become negative, or a safety limit is reached. The design of our study is aimed at: a) determining if CRT targeted resuscitation is associated with less fluid resuscitation and fluid balances; b) determining if this strategy is associated with less organ dysfunctions; and c) if it results in similar improvement in markers of tissue hypoperfusion or hypoxia such as hepato-splanchnic blood flow or microcirculatory perfusion.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Jun 2018
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
June 1, 2018
CompletedFirst Submitted
Initial submission to the registry
November 26, 2018
CompletedFirst Posted
Study publicly available on registry
December 3, 2018
CompletedPrimary Completion
Last participant's last visit for primary outcome
September 30, 2019
CompletedStudy Completion
Last participant's last visit for all outcomes
December 31, 2019
CompletedDecember 3, 2018
November 1, 2018
1.3 years
November 26, 2018
November 29, 2018
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Amount of resuscitation fluids
The total amount of fluids administered as fluid challenges from baseline to 6 hours after starting protocol
at six hours
Secondary Outcomes (7)
Total fluid balance
at 24 hours
Multiple organ dysfunction
At 24 hours, 48 hours and 72 hours
Sublingual microcirculation
at baseline, 6 hours and 24 hours
Hepato-splanchnic blood flow
At baseline, 6 hours and 24 hours
Muscle tissue oxygenation
At baseline, 6 hours and 24 hours
- +2 more secondary outcomes
Study Arms (2)
CRT guided resuscitation
EXPERIMENTALFluid resuscitation will be aimed at normalizing capillary refill time (CRT) during the intervention period. Fluid challenges will be administered at a rate of 500 ml of crystalloids over 30 minutes, with reassessment of CRT until achieving normal values, or the patient becomes fluid unresponsive, or a safety issue develops.
Lactate guided resuscitation
ACTIVE COMPARATORFluid resuscitation will be aimed at normalizing or decreasing lactate levels by more than 20% every 2 hours during the intervention during the intervention period. Fluid challenges will be administered at a rate of 500 ml of crystalloids over 30 minutes, with reassessment of lactate every 2 hours until reaching target, or the patient becomes fluid unresponsive, or a safety issue develops.
Interventions
Sequential approach with fluids (guided by dynamic predictors of fluid responsiveness), according to capillary refill time (CRT)
Sequential approach with fluids (guided by dynamic predictors of fluid responsiveness), according to lactate levels
Eligibility Criteria
You may qualify if:
- Septic shock diagnosed at ICU admission according to the Sepsis-3 Consensus Conference \[35\], basically septic patients with hypotension requiring norepinephrine (NE) to maintain a mean arterial pressure (MAP) of 65 mmHg, and serum lactate levels \> 2 mmol/l after initial fluid resuscitation.
- Less than 24 h after fulfilling criteria for septic shock
- Positive fluid responsiveness assessment
You may not qualify if:
- \. Pregnancy
- Anticipated surgery or dialytic procedure during the first 6h after septic shock diagnosis
- Do-not-resuscitate status
- Child B or C liver cirrhosis
- Active bleeding
- Severe concomitant acute respiratory distress syndrome (ARDS)
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Pontificia Universidad Catolica de Chile
Santiago, Santiago Metropolitan, 7500000, Chile
Related Publications (39)
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PMID: 23740284RESULTOspina-Tascon GA, Bautista-Rincon DF, Umana M, Tafur JD, Gutierrez A, Garcia AF, Bermudez W, Granados M, Arango-Davila C, Hernandez G. Persistently high venous-to-arterial carbon dioxide differences during early resuscitation are associated with poor outcomes in septic shock. Crit Care. 2013 Dec 13;17(6):R294. doi: 10.1186/cc13160.
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PMID: 33140173DERIVED
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Glenn Hernandez, PhD
Pontificia Universidad Catolica de Chile
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Titular Professor
Study Record Dates
First Submitted
November 26, 2018
First Posted
December 3, 2018
Study Start
June 1, 2018
Primary Completion
September 30, 2019
Study Completion
December 31, 2019
Last Updated
December 3, 2018
Record last verified: 2018-11