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Fluids in Septic Shock (FISSH) (FISSH)

Primary Purpose

Sepsis, Septic Shock

Status
Recruiting
Phase
Phase 2
Locations
International
Study Type
Interventional
Intervention
higher chloride crystalloid
lower chloride crystalloid
Sponsored by
McMaster University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Sepsis, Septic Shock

Eligibility Criteria

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

Inclusion Criteria:

  • patients 16 years or greater who meet all of the following:
  • require fluid resuscitation for refractory hypotension (systolic blood pressure <90 mmHg or mean arterial blood pressure<65 mmHg after 1 Litre bolus over 1 hour or less or organ hypo-perfusion (serum lactate >4 mmol/L)
  • have a clinical suspicion of infection
  • are within 6 hours of hospital admission or critical care response team consultation
  • are anticipated to require ICU admission

Exclusion Criteria:

  • intracranial bleed or intracranial hypertension during the index hospital admission
  • 10% of body surface area acute burn injury
  • bleeding/hemorrhage as likely cause of hypotension
  • a lack of commitment to life support
  • have previously enrolled in FISSH, or a confounding trial (e.g. a trial examining the effect of other intravenous fluids in septic shock patients)
  • been transferred from another hospital or facility >6 hours since presentation to first hospital
  • pre-established end stage renal disease (ESRD) or are receiving hemodialysis (intermittent or continuous) at time of enrolment, or
  • been admitted to ICU directly from the operating room or post anaesthetic care unit

Sites / Locations

  • University of Calgary - Foothills Medical CentreRecruiting
  • University of Calgary - Rockyview General HospitalRecruiting
  • Grey Nuns Community HospitalRecruiting
  • Halifax InfirmaryRecruiting
  • Victoria GeneralRecruiting
  • Brantford General HospitalRecruiting
  • St Joseph's HealthcareRecruiting
  • Juravinski Hospital-Hamilton Health SciencesRecruiting
  • Hamilton General HospitalRecruiting
  • Kingston General HospitalRecruiting
  • London Health Sciences Centre - Victoria HospitalRecruiting
  • London Health Sciences - University HospitalRecruiting
  • Lakeridge HealthRecruiting
  • Niagara Health, St Catharines SiteRecruiting
  • Unity Health (St. Michael's Hospital)Recruiting
  • Mount Sinai HospitalRecruiting
  • Sunnybrook Health Sciences CentreRecruiting
  • Centre intégré Universitaire de santé et de services sociaux du Nord de l'île de MontréalRecruiting
  • Centre Hospitalier de l'Universite de Montreal (CHUM)Recruiting
  • Centre de recherche du CIUSSS de l'Estrie - CHUS de SherbrookeRecruiting
  • Centre intégré universitaire de santé et de services sociaux de la Mauricie-et-du-Centre-du-Québec (CIUSSS MCQ)Recruiting
  • King Abdulaziz Medical City- Riyadh (KAMC-R)Recruiting
  • King Faisal Specialist Hospital & Research CentreRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

higher chloride solutions

lower chloride solutions

Arm Description

higher chloride crystalloid (Normal saline - chloride concentration 154 mmol/L)

lower chloride crystalloid (Ringer's lactate - chloride concentration 110 mmol/L)

Outcomes

Primary Outcome Measures

30-day Mortality
We expect that if a difference in survival is demonstrated, that this will be evident within 30 days

Secondary Outcome Measures

Acute Kidney Injury
Development of stage 2 or worse acute kidney injury (AKI) according to KIDGO guidelines on serum creatinine criteria

Full Information

First Posted
August 27, 2018
Last Updated
September 25, 2023
Sponsor
McMaster University
Collaborators
The Physicians' Services Incorporated Foundation, Canadian Institutes of Health Research (CIHR)
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1. Study Identification

Unique Protocol Identification Number
NCT03677102
Brief Title
Fluids in Septic Shock (FISSH)
Acronym
FISSH
Official Title
Fluids in Septic Shock (FISSH): a Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
September 2023
Overall Recruitment Status
Recruiting
Study Start Date
September 9, 2018 (Actual)
Primary Completion Date
November 28, 2025 (Anticipated)
Study Completion Date
December 31, 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
McMaster University
Collaborators
The Physicians' Services Incorporated Foundation, Canadian Institutes of Health Research (CIHR)

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Despite evidence of the physiologic benefits and possible lower mortality associated with low chloride solutions, normal saline remains the most wildly used fluid in the world. Given uncertainty about the impact of lower chloride versus higher chloride solutions on mortality, it is unlikely that clinical practice will change without new and direct randomized controlled trial (RCT) evidence. Editorials published in leading critical care journals have called for RCT's to address this important clinical question. This trial will directly compare low chloride versus normal chloride for resuscitation in septic shock on patient-important outcomes such as mortality and AKI.
Detailed Description
Severe infection can lead to many complications within the human body including low blood pressure, which is called septic shock. The main treatments for septic shock are intravenous antibiotics and intravenous fluid. There are many different intravenous fluids available for doctors to use. Each one of these fluids has potential advantages as well as potential disadvantages. Doctors will often look at many things when deciding which fluid to give including the results of bloodwork and the clinical characteristics of the patients themselves. There is limited direction from research studies that using one fluid type is better than another. Some preliminary research in the field has suggested that one specific electrolyte, call chloride, may be harmful when given to patients in high concentrations. Animal research has shown that the administration of high chloride fluids may be harmful to the lungs, kidneys, gastrointestinal and muscle cells. Some intravenous fluids have higher concentrations of chloride than others. The investigators plan to study the impact of giving patients with severe infection intravenous fluids with either a high chloride concentration (normal saline or high chloride albumin) or a low chloride concentration (Ringers Lactate or low chloride albumin). This trial will build on the earlier pilot, phase 1 study and will look at patient-important outcomes such as rate of death, kidney failure and length of stay in the ICU. This larger study has the potential to guide the care of critically ill patients with infection worldwide.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Sepsis, Septic Shock

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2, Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
1096 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
higher chloride solutions
Arm Type
Active Comparator
Arm Description
higher chloride crystalloid (Normal saline - chloride concentration 154 mmol/L)
Arm Title
lower chloride solutions
Arm Type
Active Comparator
Arm Description
lower chloride crystalloid (Ringer's lactate - chloride concentration 110 mmol/L)
Intervention Type
Other
Intervention Name(s)
higher chloride crystalloid
Intervention Description
Normal saline (chloride concentration 154 mmol/L)
Intervention Type
Other
Intervention Name(s)
lower chloride crystalloid
Intervention Description
Ringer's Lactate (chloride concentration 110 mmol/L)
Primary Outcome Measure Information:
Title
30-day Mortality
Description
We expect that if a difference in survival is demonstrated, that this will be evident within 30 days
Time Frame
up to 30 days
Secondary Outcome Measure Information:
Title
Acute Kidney Injury
Description
Development of stage 2 or worse acute kidney injury (AKI) according to KIDGO guidelines on serum creatinine criteria
Time Frame
up to 30 days
Other Pre-specified Outcome Measures:
Title
Hospital/ICU length of stay
Description
length of hospital/ICU stay up to 30 days
Time Frame
up to 30 days
Title
Ventilator free days
Description
Number of ventilator free days
Time Frame
censored at 30 days
Title
Number of days requiring vasoactive agents
Description
defined as the number of days requiring great than or equal to 2 hours of intravenous vasopressor support
Time Frame
up to 30 days
Title
Incidence of biochemical abnormalities during study period
Description
any serum blood test results showing hyperchloremia, hyperkalemia, hypernatremia, or acidosis
Time Frame
up to 30 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
16 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: patients 16 years or greater who meet all of the following: require fluid resuscitation for refractory hypotension (systolic blood pressure <90 mmHg or mean arterial blood pressure<65 mmHg after 1 Litre bolus over 1 hour or less or organ hypo-perfusion (serum lactate >4 mmol/L) have a clinical suspicion of infection are within 6 hours of hospital admission or critical care response team consultation are anticipated to require ICU admission Exclusion Criteria: intracranial bleed or intracranial hypertension during the index hospital admission 10% of body surface area acute burn injury bleeding/hemorrhage as likely cause of hypotension a lack of commitment to life support have previously enrolled in FISSH, or a confounding trial (e.g. a trial examining the effect of other intravenous fluids in septic shock patients) been transferred from another hospital or facility >6 hours since presentation to first hospital pre-established end stage renal disease (ESRD) or are receiving hemodialysis (intermittent or continuous) at time of enrolment, or been admitted to ICU directly from the operating room or post anaesthetic care unit
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Bram Rochwerg, MSc,MD,FRCPC
Phone
905-521-2100
Ext
42442
Email
rochwerg@mcmaster.ca
First Name & Middle Initial & Last Name or Official Title & Degree
Peggy Austin
Phone
905-525-9140
Ext
22154
Email
austinp@hhsc.ca
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Bram Rochwerg, MSc,MD,FRCPC
Organizational Affiliation
McMaster University
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Calgary - Foothills Medical Centre
City
Calgary
State/Province
Alberta
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Lois Hagan, CRA
Phone
(403)-944-2160
Email
lois.hagan@ucalgary.ca
First Name & Middle Initial & Last Name & Degree
Ken Parhar, MD MSc FRCPC
Facility Name
University of Calgary - Rockyview General Hospital
City
Calgary
State/Province
Alberta
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Lois Hagan, CRA
Phone
(403)-944-2160
Email
lois.hagan@ucalgary.ca
First Name & Middle Initial & Last Name & Degree
Ken Parhar, MD MSc FRCPC
Facility Name
Grey Nuns Community Hospital
City
Edmonton
State/Province
Alberta
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Anushka Jayasekara, RC
Email
Anushka.Jayasekara@covenanthealth.ca
First Name & Middle Initial & Last Name & Degree
Janek Senaratne, MD,MSc,ABIM,FRCPC,FACC,FESC
First Name & Middle Initial & Last Name & Degree
Lazar Milovanovic, MD,FRCPC
Facility Name
Halifax Infirmary
City
Halifax
State/Province
Nova Scotia
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Linda Hasties, RN, BHScN
Phone
902-499-9225
Email
Linda.Hastie@nshealth.ca
First Name & Middle Initial & Last Name & Degree
Osama Loubani, MD,FRCPC,DABEM
First Name & Middle Initial & Last Name & Degree
Stephen Beed, MD, FRCPC
First Name & Middle Initial & Last Name & Degree
Volker Eichhorn, MD
First Name & Middle Initial & Last Name & Degree
Robert Green, MD, FRCPC
First Name & Middle Initial & Last Name & Degree
Jennifer Hancock, MD, FRCP
First Name & Middle Initial & Last Name & Degree
Babar Haroon, MD, FRCPC
First Name & Middle Initial & Last Name & Degree
Sarah McMullen, MD, FRCPC
First Name & Middle Initial & Last Name & Degree
Samuel Minor, MD, FRCSC
First Name & Middle Initial & Last Name & Degree
Laurel Murphy, MD, FRCPC
First Name & Middle Initial & Last Name & Degree
Tony O'Leary, MD, FRCP
First Name & Middle Initial & Last Name & Degree
Patrick Ward, MD, FRCP
First Name & Middle Initial & Last Name & Degree
Jack Rasmussen, MD, FRCSC
First Name & Middle Initial & Last Name & Degree
Edmund Chong-How (Edmund) Tan, MD, FRCPC
First Name & Middle Initial & Last Name & Degree
Tobias Witter, MD
Facility Name
Victoria General
City
Halifax
State/Province
Nova Scotia
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Linda Hastie, RN, BHScN
Phone
902-499-9225
Email
Linda.Hastie@nshealth.ca
First Name & Middle Initial & Last Name & Degree
Osama Loubani, MD,FRCPC,DABEM
First Name & Middle Initial & Last Name & Degree
Stephen Beed, MD, FRCPC
First Name & Middle Initial & Last Name & Degree
Volker Eichhorn, MD
First Name & Middle Initial & Last Name & Degree
Robert Green, MD, FRCPC
First Name & Middle Initial & Last Name & Degree
Jennifer Hancock, MD, FRCP
First Name & Middle Initial & Last Name & Degree
Babar Haroon, MD, FRCPC
First Name & Middle Initial & Last Name & Degree
Sarah McMullen, MD, FRCPC
First Name & Middle Initial & Last Name & Degree
Samuel Minor, MD, FRCSC
First Name & Middle Initial & Last Name & Degree
Laurel Murphy, MD, FRCPC
First Name & Middle Initial & Last Name & Degree
Tony O'Leary, MD, FRCP
First Name & Middle Initial & Last Name & Degree
Patrick Ward, MD, FRCP
First Name & Middle Initial & Last Name & Degree
Jack Rasmussen, MD, FRCSC
First Name & Middle Initial & Last Name & Degree
Edmund Chong-How (Edmund) Tanter, MD, FRCPC
First Name & Middle Initial & Last Name & Degree
Tobias Witter, MD
Facility Name
Brantford General Hospital
City
Brantford
State/Province
Ontario
ZIP/Postal Code
N3R 1G9
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
William Dechert, MSc
Phone
519-752-7871
Ext
4531
Email
wdechert@stjosham.on.ca
First Name & Middle Initial & Last Name & Degree
Brenda Reeve, MD, FRCPC
Facility Name
St Joseph's Healthcare
City
Hamilton
State/Province
Ontario
ZIP/Postal Code
L8N 4A6
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
France Clarke, RRT
Phone
905-522-1155
Ext
33633
Email
clarkef@mcmaster.ca
First Name & Middle Initial & Last Name & Degree
Deborah J Cook, MD,FRCPC,MSc
Facility Name
Juravinski Hospital-Hamilton Health Sciences
City
Hamilton
State/Province
Ontario
ZIP/Postal Code
L8V 1C1
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Bram Rochwerg, MSc,MD,FRCPC
Phone
905-521-2100
Ext
42442
Email
rochwerg@mcmaster.ca
First Name & Middle Initial & Last Name & Degree
Tina Millen, RRT
Phone
905-719-6133
Email
millent@mcmaster.ca
First Name & Middle Initial & Last Name & Degree
Bram Rochwerg, MSc,MD,FRCPC
Facility Name
Hamilton General Hospital
City
Hamilton
State/Province
Ontario
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Lori Hand, RRT
Email
handlori@HHSC.CA
First Name & Middle Initial & Last Name & Degree
Maureen Meade, MD,FRCPC,MSc
Facility Name
Kingston General Hospital
City
Kingston
State/Province
Ontario
ZIP/Postal Code
K7L 2V7
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Tracy Boyd, CCRC
Phone
613-549-6666
Ext
2608
Email
Tracy.Boyd@kingstonhsc.ca
First Name & Middle Initial & Last Name & Degree
Gordon Boyd, MD,PhD,FRCPC
Facility Name
London Health Sciences Centre - Victoria Hospital
City
London
State/Province
Ontario
ZIP/Postal Code
N6A 5W9
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Eileen Campbell, RN
Phone
519-685-8500
Ext
55664
Email
Eileen.Campbell@lhsc.on.ca
First Name & Middle Initial & Last Name & Degree
Ian Ball, MC,MSc,FRCPC
First Name & Middle Initial & Last Name & Degree
Marat Slessarev, MD, FRCPC
Facility Name
London Health Sciences - University Hospital
City
London
State/Province
Ontario
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Tracey C Bentall
Email
TraceyC.Bentall@lhsc.on.ca
First Name & Middle Initial & Last Name & Degree
Eileen Campbell
Email
Eileen.Campbell@lhsc.on.ca
First Name & Middle Initial & Last Name & Degree
Ian Ball, MD,MSc(Epi),FRCPC
First Name & Middle Initial & Last Name & Degree
John Basmaji, MD,FRCPC
Facility Name
Lakeridge Health
City
Oshawa
State/Province
Ontario
ZIP/Postal Code
L1G 2B9
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Barbara Flynn, RN BScN
Email
bflynn@lh.ca
First Name & Middle Initial & Last Name & Degree
Sarah Dulmage, ScH
Email
sdulmage@lh.ca
First Name & Middle Initial & Last Name & Degree
Shannon Fernando, MD,MSc,FRCPC
First Name & Middle Initial & Last Name & Degree
Karim Soliman, MD,FRCPC
First Name & Middle Initial & Last Name & Degree
Kavita Sridhar, MD,MHSc,FRCPC
Facility Name
Niagara Health, St Catharines Site
City
St Catharines
State/Province
Ontario
ZIP/Postal Code
L2S 0A9
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Lisa Patterson, RC
Email
Lisa.Patterson@niagarahealth.on.ca
First Name & Middle Initial & Last Name & Degree
Erick Duan, MD, FRCPC
First Name & Middle Initial & Last Name & Degree
Jennifer Tsang, MD,PhD,FRCPC
Facility Name
Unity Health (St. Michael's Hospital)
City
Toronto
State/Province
Ontario
ZIP/Postal Code
M5B 1W8
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Marlene Santos, MD, ACRP
Phone
416-864-6060
Ext
2322
Email
Marlene.Santos@unityhealth.to
First Name & Middle Initial & Last Name & Degree
Karen E Burns, MD,FRCPC
First Name & Middle Initial & Last Name & Degree
Jan Friedrich, MD, PhD, MSc
Facility Name
Mount Sinai Hospital
City
Toronto
State/Province
Ontario
ZIP/Postal Code
M5G 1X5
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Sumesh Shah, CCRP
Phone
416-586-4800
Ext
8445
Email
Sumesh.Shah@SinaiHealthSystem.ca
First Name & Middle Initial & Last Name & Degree
SANGEETA MEHTA, MD,FRCPC
Facility Name
Sunnybrook Health Sciences Centre
City
Toronto
State/Province
Ontario
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Nicole Marinoff, RN, CCRP
Email
Nicole.Marinoff@sunnybrook.ca
First Name & Middle Initial & Last Name & Degree
Neill Adhikari, MDCM, MSc.
Facility Name
Centre intégré Universitaire de santé et de services sociaux du Nord de l'île de Montréal
City
Montreal
State/Province
Quebec
ZIP/Postal Code
H4J 1C5
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Virginie Williams, PhD
Phone
514 338 2222
Ext
583-3272
Email
virginie.williams.cnmtl@ssss.gouv.qc.ca
First Name & Middle Initial & Last Name & Degree
Karim Serri, BSc,MD
Facility Name
Centre Hospitalier de l'Universite de Montreal (CHUM)
City
Montréal
State/Province
Quebec
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Andrea Gagnon-Hamelin
Email
andrea.gagnon-hamelin.chum@ssss.gouv.qc.ca
First Name & Middle Initial & Last Name & Degree
Emmanuel Charbonney, MD, PhD
Facility Name
Centre de recherche du CIUSSS de l'Estrie - CHUS de Sherbrooke
City
Sherbrooke
State/Province
Quebec
ZIP/Postal Code
J1H 5N4
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Marie-Pier Bouchard, RA
Email
marie-pier.bouchard.ciussse-chus@ssss.gouv.qc.ca
First Name & Middle Initial & Last Name & Degree
François Lamontagne, MD,MSc
First Name & Middle Initial & Last Name & Degree
Fred D'aragon, MD, MSc
Facility Name
Centre intégré universitaire de santé et de services sociaux de la Mauricie-et-du-Centre-du-Québec (CIUSSS MCQ)
City
Trois-Rivières
State/Province
Quebec
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Alice Lefebvre, RC
Phone
819 697-3333
Ext
64820
Email
alice.lefebvre@ssss.gouv.qc.ca
First Name & Middle Initial & Last Name & Degree
Jean-Francois Naud, MD
Facility Name
King Abdulaziz Medical City- Riyadh (KAMC-R)
City
Riyadh
Country
Saudi Arabia
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Felwa Bin Humaid, BSc
First Name & Middle Initial & Last Name & Degree
Sara Aldekhyl, MBBS,ABIM,FRCPc,MedEd
Facility Name
King Faisal Specialist Hospital & Research Centre
City
Riyadh
Country
Saudi Arabia
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Samar Nouri, CRC
Email
snouri@kfhrc.edu.sa
First Name & Middle Initial & Last Name & Degree
Zainab Al Duhailib, MD

12. IPD Sharing Statement

Learn more about this trial

Fluids in Septic Shock (FISSH)

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