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Senolytic
Fisetin for Sepsis
Phase 2
Recruiting
Led By Michael Puskarich, MD
Research Sponsored by University of Minnesota
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up day 28
Summary
This trial will test if a drug called fisetin helps reduce the risk of sepsis in older people.
Who is the study for?
The STOP-Sepsis trial is for people aged 65 or older who are hospitalized with a primary diagnosis of acute infection and expected to stay at least 48 hours. They must have a certain level of organ dysfunction but not severe kidney failure, very low blood counts, invasive fungal infections, or be in intensive care.
What is being tested?
This study tests different doses of Fisetin against a placebo to see if they can reduce the severity of sepsis in older patients by targeting aging cells. It's set up so that more successful treatments get tested on more patients as the trial goes on.
What are the potential side effects?
Potential side effects aren't specified here, but generally could include allergic reactions to Fisetin, possible interactions with other medications being taken, and typical drug-related risks like nausea or headaches.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ day 28
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~day 28
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Difference in the composite cardiovascular, respiratory, and renal sequential organ failure assessment (CRR-SOFA)
Secondary study objectives
All-cause mortality
Days in the ICU
Organ failure free days
+7 moreTrial Design
3Treatment groups
Experimental Treatment
Placebo Group
Group I: Fisetin- dose 2Experimental Treatment1 Intervention
Elderly (\>=65 years) patients admitted to the hospital with an acute infection and sequential organ failure assessment score sufficient for a diagnosis of sepsis, will be given the 2nd does of fisetin.
Group II: Fisetin- dose 1Experimental Treatment1 Intervention
Elderly (\>=65 years) patients admitted to the hospital with an acute infection and sequential organ failure assessment score sufficient for a diagnosis of sepsis, will be given the first dose of fisetin.
Group III: PlaceboPlacebo Group1 Intervention
Elderly (\>=65 years) patients admitted to the hospital with an acute infection and sequential organ failure assessment score sufficient for a diagnosis of sepsis will receive placebo treatment.
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Who is running the clinical trial?
University of MinnesotaLead Sponsor
1,427 Previous Clinical Trials
1,620,353 Total Patients Enrolled
Michael Puskarich, MDPrincipal InvestigatorUniversity of Minnesota
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I have been diagnosed with HIV, Hepatitis B, or Hepatitis C.My kidney function is severely reduced.I do not have uncontrolled fluid buildup as judged by my doctor.I am currently on life support treatments like dialysis or a ventilator.I am receiving palliative care focused on comfort.I have been admitted to the ICU.I have been admitted to the hospital.I am currently on medication that may interact with other drugs.I have a new or active cancer, not including non-melanoma skin cancers.I am 65 years old or older.I have been diagnosed with an acute infection.
Research Study Groups:
This trial has the following groups:- Group 1: Fisetin- dose 1
- Group 2: Fisetin- dose 2
- Group 3: Placebo
Awards:
This trial has 0 awards, including:Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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